Impulse™

158 catalogue numbers from H74916599230, listed by Boston Scientific Corporation, United States, under Catheter, Intravascular, Diagnostic. 11 manufacturers in China are registered for this product code.

Registry build 21.09.26
11manufacturers in China registered for this device type
158catalogue numbers in this listing
20510(k) clearances naming this product code
40recalls on this code

Who Else Makes It

Concentrated in Jiangsu (5), Guangdong (3), Zhejiang (2). 4 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code DQO
Manufacturer City Province Registered as Device types
GE Medical Systems (China) Co., Ltd. Wuxi Jiangsu Contract manufacturer 57
Amsino Medical (Kunshan) Co., Ltd. Kunshan Jiangsu Contract manufacturer 53
Conod Medical Shuyang Co., Ltd. Shuyang Jiangsu Contract manufacturer 22
Bioxin Medical Co., Ltd. Weihai Shandong Contract manufacturer 8
GRI Medical & Electronic Technology Co., Ltd. Jiaxing Zhejiang Contract manufacturer 71
Goals Sterilization Co., Ltd. Jiaxing Zhejiang Contract manufacturer 26
Wuxi Goals Medical Technology Co., Ltd. Yixing Jiangsu Contract manufacturer 24
Sunny Medical Device (Shenzhen) Co., Ltd. Shenzhen Guangdong Contract manufacturer 11
Curatia Medical Limited Suzhou Jiangsu Specification developer 5
Shenzhen Vivolight Medical Device&Technology Co., Ltd. Shenzhen Guangdong Manufacturer 4
Shenzhen Antmed Co., Ltd. Dongguan Guangdong Manufacturer 4

Record

Regulatory record for Impulse™
Listed by Boston Scientific Corporation, United States
FDA product code DQO
Device type Catheter, Intravascular, Diagnostic
Device class Class 2
Regulation 21 CFR 870.1200
Establishment Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer, Exporter
Record published 2016-09-24
Record revised 2018-03-29 (version 2)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Supplied as a kit Yes
Label carries lot or batch number, expiry date
Packaging Pack of 5

Catalogue Numbers

Catalogue numbers for Impulse™
Catalogue number Size Status
H74916599230 6 F Diameter In distribution
H749165991620 2.1 mm Diameter In distribution
H749163912011 1.70 mm Diameter In distribution
H74916599210 2.1 mm Diameter In distribution
H74916599450 2.1 mm Diameter In distribution
H749165991420 6 F Diameter In distribution
H74916599220 6 F Diameter In distribution
H749165991530 6 F Diameter In distribution
H749165991630 6 F Diameter In distribution
H7491639120B1 1.70 mm Diameter In distribution
H74916391251 5 F Diameter In distribution
H74916599500A0 6 F Diameter In distribution
H749165992400 2.1 mm Diameter In distribution
H749165992511 2.1 mm Diameter In distribution
H749163911741 5 F Diameter In distribution
H7491639121C1 1.70 mm Diameter In distribution
H7491639102J1 5 F Diameter In distribution
H7491639189A1 5 F Diameter In distribution
H74916391421 5 F Diameter In distribution
H749165992020 2.1 mm Diameter In distribution
H74916391041 5 F Diameter In distribution
H74916599980 6 F Diameter In distribution
H749163912201 1.70 mm Diameter In distribution
H749165991510 2.1 mm Diameter In distribution
H749163911711 5 F Diameter In distribution
H74916599840 2.1 mm Diameter In distribution
H749165992300 6 F Diameter In distribution
H74916391375A1 5 F Diameter In distribution
H749165991210 2.1 mm Diameter In distribution
H74916599960 6 F Diameter In distribution
H749163912021 1.70 mm Diameter In distribution
H749165992010 2.1 mm Diameter In distribution
H74916391431 1.70 mm Diameter In distribution
H74916599030 6 F Diameter In distribution
H749163912411 1.70 mm Diameter In distribution
H749163911621 5 F Diameter In distribution
H74916391188A1 5 F Diameter In distribution
H749163912531 1.70 mm Diameter In distribution
H749163912151 1.70 mm Diameter In distribution
H749163913001 5 F Diameter In distribution
H749165991800 6 F Diameter In distribution
H749163912251 1.70 mm Diameter In distribution
H749165995050 6 F Diameter In distribution
H74916391174C1 5 F Diameter In distribution
H749165991900 2.1 mm Diameter In distribution
H74916391202B1 1.70 mm Diameter In distribution
H749163912031 5 F Diameter In distribution
H74916599240 2.1 mm Diameter In distribution
H749165992030 2.1 mm Diameter In distribution
H7491639150A1 1.70 mm Diameter In distribution
H749163912501 5 F Diameter In distribution
H749163913021 1.70 mm Diameter In distribution
H749163915011 5 F Diameter In distribution
H74916391891 1.70 mm Diameter In distribution
H749165992250 6 F Diameter In distribution
H74916391051 5 F Diameter In distribution
H74916599172A0 2.1 mm Diameter In distribution
H74916599430 2.1 mm Diameter In distribution
H749163915001 1.70 mm Diameter In distribution
H749165992200 2.1 mm Diameter In distribution
H749165991610 2.1 mm Diameter In distribution
H749163911531 1.70 mm Diameter In distribution
H74916391841 1.70 mm Diameter In distribution
H74916599573A0 2.1 mm Diameter In distribution
H749165991710 2.1 mm Diameter In distribution
H749163912401 5 F Diameter In distribution
H749163911611 5 F Diameter In distribution
H74916599574A0 6 F Diameter In distribution
H749165993010 2.1 mm Diameter In distribution
H74916391330A1 5 F Diameter In distribution
H74916599698A0 6 F Diameter In distribution
H74916599252 2.1 mm Diameter In distribution
H749163911421 1.70 mm Diameter In distribution
H749163911221 1.70 mm Diameter In distribution
H749163915051 5 F Diameter In distribution
H749165993000 2.1 mm Diameter In distribution
H749165991460 2.1 mm Diameter In distribution
H74916391203A1 1.70 mm Diameter In distribution
H74916391187A1 1.70 mm Diameter In distribution
H749163911211 1.70 mm Diameter In distribution
H74916391441 5 F Diameter In distribution
H749165992531 2.1 mm Diameter In distribution
H74916391211 1.70 mm Diameter In distribution
H74916391305A1 1.70 mm Diameter In distribution
H749165991740 6 F Diameter In distribution
H74916391401 5 F Diameter In distribution
H74916391185A1 1.70 mm Diameter In distribution
H74916599440 6 F Diameter In distribution
H7491659920A0 6 F Diameter In distribution
H749163911171 5 F Diameter In distribution
H74916391201E1 1.70 mm Diameter In distribution
H74916391961 1.70 mm Diameter In distribution
H7491639120A1 1.70 mm Diameter In distribution
H74916391174B1 1.70 mm Diameter In distribution
H74916599575A0 6 F Diameter In distribution
H749163912351 1.70 mm Diameter In distribution
H749163911521 5 F Diameter In distribution
H749163912301 5 F Diameter In distribution
H749165995040 2.1 mm Diameter In distribution
H74916599330A0 2.1 mm Diameter In distribution
H74916599400 6 F Diameter In distribution
H749163911731 1.70 mm Diameter In distribution
H74916391861 5 F Diameter In distribution
H74916391221 5 F Diameter In distribution
H749163913011 1.70 mm Diameter In distribution
H74916599102A0 2.1 mm Diameter In distribution
H74916391117B1 5 F Diameter In distribution
H749163912521 1.70 mm Diameter In distribution
H74916599420 2.1 mm Diameter In distribution
H749163915041 1.70 mm Diameter In distribution
H74916391021 1.70 mm Diameter In distribution
H7491659925A0 2.1 mm Diameter In distribution
H7491639101A1 1.70 mm Diameter In distribution
H74916391241 5 F Diameter In distribution
H74916599020 6 F Diameter In distribution
H749165992521 6 F Diameter In distribution
H749165993020 2.1 mm Diameter In distribution
H749165991000 2.1 mm Diameter In distribution
H749165991220 6 F Diameter In distribution
H749165995010 2.1 mm Diameter In distribution
H7491639196A1 1.70 mm Diameter In distribution
H74916391411 5 F Diameter In distribution
H74916599576A0 6 F Diameter In distribution
H74916599890 2.1 mm Diameter In distribution
H74916599860 2.1 mm Diameter In distribution
H749163912511 5 F Diameter In distribution
H74916599250 2.1 mm Diameter In distribution
H749165995000 2.1 mm Diameter In distribution
H74916391123A1 1.70 mm Diameter In distribution
H749163911801 1.70 mm Diameter In distribution
H749165992150 2.1 mm Diameter In distribution
H74916391031 1.70 mm Diameter In distribution
H74916391231 1.70 mm Diameter In distribution
H74916599040 2.1 mm Diameter In distribution
H74916391174D1 5 F Diameter In distribution
H749163911511 1.70 mm Diameter In distribution
H749165991730 2.1 mm Diameter In distribution
H74916391174E1 5 F Diameter In distribution
H74916391981 1.70 mm Diameter In distribution
H749163915021 5 F Diameter In distribution
H749165992350 6 F Diameter In distribution
H74916391011 5 F Diameter In distribution
H74916391142B1 5 F Diameter In distribution
H749163911951 1.70 mm Diameter In distribution
H749165995030 6 F Diameter In distribution
H749165995020 6 F Diameter In distribution
H74916599010 6 F Diameter In distribution
H74916599410 6 F Diameter In distribution
H74916599050 6 F Diameter In distribution
H749165991170 2.1 mm Diameter In distribution
H749163911461 1.70 mm Diameter In distribution
H749165991950 6 F Diameter In distribution
H749165992501 2.1 mm Diameter In distribution
H7491659941C0 2.1 mm Diameter In distribution
H7491639198A1 1.70 mm Diameter In distribution
H749163911901 1.70 mm Diameter In distribution
H74916391320A1 1.70 mm Diameter In distribution
H749163911001 1.70 mm Diameter In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Performa® Merit Medical Systems, Inc. 1,101
Impress® Merit Medical Systems, Inc. 839
Super Torque Cordis Corp. 611
Soft-Vu AngioDynamics, Inc. 591
Torcon NB Cook Incorporated 463
Mariner AngioDynamics, Inc. 323
INT,SlideCath Shanghai Kindly Medical Instruments Co., Ltd. 264
Infiniti Cordis Corp. 251
Infiniti Cordis US Corp. 241
AngiOptic AngioDynamics, Inc. 227
Tempo Cordis Corp. 217
SiteSeer™ Medtronic, Inc. 204

Showing 12 of 226. All products under Catheter, Intravascular, Diagnostic

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K152605 2015-10-29
K121694 2012-09-14
K120495 2012-05-21
K120893 2012-03-29
K063312 2006-11-30
K060175 2006-03-24
K050863 2005-09-02
K050684 2005-05-20
K050577 2005-03-30
K040776 2004-04-29
K023681 2002-11-26
K022621 2002-09-04
K970207 1997-07-31
K971607 1997-07-24
K953114 1995-09-12
K942927 1995-06-13
K913871 1991-11-25
K904788 1990-12-17
K895542 1990-04-06
K891580 1989-08-03

Recalls

40 of these are Class I. Class I is the FDA’s most serious grade: a reasonable probability of serious injury or death. Volume alone is not a quality signal: a manufacturer that ships more recalls more.

Recalls referencing this product code
Initiated FDA class Root cause Reason Quantity
2024-03-21 Class I Under Investigation by firm An increase in complaints related to an inability to advance the guidewire through the lumen of the device for certain batches. There is evidence of the polyurethane layer delaminating and in some instances material detachment in the cathet 37252 catheters
2024-03-21 Class I Under Investigation by firm An increase in complaints related to an inability to advance the guidewire through the lumen of the device for certain batches. There is evidence of the polyurethane layer delaminating and in some instances material detachment in the cathet 263522 catheters
2024-03-21 Class I Under Investigation by firm An increase in complaints related to an inability to advance the guidewire through the lumen of the device for certain batches. There is evidence of the polyurethane layer delaminating and in some instances material detachment in the cathet 615 catheters
2024-03-21 Class I Under Investigation by firm An increase in complaints related to an inability to advance the guidewire through the lumen of the device for certain batches. There is evidence of the polyurethane layer delaminating and in some instances material detachment in the cathet 8715 catheters
2024-03-21 Class I Under Investigation by firm An increase in complaints related to an inability to advance the guidewire through the lumen of the device for certain batches. There is evidence of the polyurethane layer delaminating and in some instances material detachment in the cathet 1669 catheters
2024-03-21 Class I Under Investigation by firm An increase in complaints related to an inability to advance the guidewire through the lumen of the device for certain batches. There is evidence of the polyurethane layer delaminating and in some instances material detachment in the cathet 385 catheters
2024-03-21 Class I Under Investigation by firm An increase in complaints related to an inability to advance the guidewire through the lumen of the device for certain batches. There is evidence of the polyurethane layer delaminating and in some instances material detachment in the cathet 363 catheters
2024-03-21 Class I Under Investigation by firm An increase in complaints related to an inability to advance the guidewire through the lumen of the device for certain batches. There is evidence of the polyurethane layer delaminating and in some instances material detachment in the cathet 230 catheters
2024-03-21 Class I Under Investigation by firm An increase in complaints related to an inability to advance the guidewire through the lumen of the device for certain batches. There is evidence of the polyurethane layer delaminating and in some instances material detachment in the cathet 3127 catheters
2024-03-21 Class I Under Investigation by firm An increase in complaints related to an inability to advance the guidewire through the lumen of the device for certain batches. There is evidence of the polyurethane layer delaminating and in some instances material detachment in the cathet 1015 catheters
2024-03-21 Class I Under Investigation by firm An increase in complaints related to an inability to advance the guidewire through the lumen of the device for certain batches. There is evidence of the polyurethane layer delaminating and in some instances material detachment in the cathet 120 catheters
2024-03-21 Class I Under Investigation by firm An increase in complaints related to an inability to advance the guidewire through the lumen of the device for certain batches. There is evidence of the polyurethane layer delaminating and in some instances material detachment in the cathet 86898 catheters
2024-03-21 Class I Under Investigation by firm An increase in complaints related to an inability to advance the guidewire through the lumen of the device for certain batches. There is evidence of the polyurethane layer delaminating and in some instances material detachment in the cathet 105 catheters
2024-03-21 Class I Under Investigation by firm An increase in complaints related to an inability to advance the guidewire through the lumen of the device for certain batches. There is evidence of the polyurethane layer delaminating and in some instances material detachment in the cathet 11109 catheters
2024-03-21 Class I Under Investigation by firm An increase in complaints related to an inability to advance the guidewire through the lumen of the device for certain batches. There is evidence of the polyurethane layer delaminating and in some instances material detachment in the cathet 16797 catheters
2024-03-21 Class I Under Investigation by firm An increase in complaints related to an inability to advance the guidewire through the lumen of the device for certain batches. There is evidence of the polyurethane layer delaminating and in some instances material detachment in the cathet 8579 catheters
2024-03-21 Class I Under Investigation by firm An increase in complaints related to an inability to advance the guidewire through the lumen of the device for certain batches. There is evidence of the polyurethane layer delaminating and in some instances material detachment in the cathet 0
2024-03-21 Class I Under Investigation by firm An increase in complaints related to an inability to advance the guidewire through the lumen of the device for certain batches. There is evidence of the polyurethane layer delaminating and in some instances material detachment in the cathet 1322 catheters
2024-03-21 Class I Under Investigation by firm An increase in complaints related to an inability to advance the guidewire through the lumen of the device for certain batches. There is evidence of the polyurethane layer delaminating and in some instances material detachment in the cathet 1065 catheters
2024-03-21 Class I Under Investigation by firm An increase in complaints related to an inability to advance the guidewire through the lumen of the device for certain batches. There is evidence of the polyurethane layer delaminating and in some instances material detachment in the cathet 116091 catheters
2024-03-21 Class I Under Investigation by firm An increase in complaints related to an inability to advance the guidewire through the lumen of the device for certain batches. There is evidence of the polyurethane layer delaminating and in some instances material detachment in the cathet 297479 catheters
2024-03-21 Class I Under Investigation by firm An increase in complaints related to an inability to advance the guidewire through the lumen of the device for certain batches. There is evidence of the polyurethane layer delaminating and in some instances material detachment in the cathet 1465 catheters
2024-03-21 Class I Under Investigation by firm An increase in complaints related to an inability to advance the guidewire through the lumen of the device for certain batches. There is evidence of the polyurethane layer delaminating and in some instances material detachment in the cathet 15270 catheters
2024-03-21 Class I Under Investigation by firm An increase in complaints related to an inability to advance the guidewire through the lumen of the device for certain batches. There is evidence of the polyurethane layer delaminating and in some instances material detachment in the cathet 290 catheters
2024-03-21 Class I Under Investigation by firm An increase in complaints related to an inability to advance the guidewire through the lumen of the device for certain batches. There is evidence of the polyurethane layer delaminating and in some instances material detachment in the cathet 15 catheters
2024-03-21 Class I Under Investigation by firm An increase in complaints related to an inability to advance the guidewire through the lumen of the device for certain batches. There is evidence of the polyurethane layer delaminating and in some instances material detachment in the cathet 46860 catheters
2024-03-21 Class I Under Investigation by firm An increase in complaints related to an inability to advance the guidewire through the lumen of the device for certain batches. There is evidence of the polyurethane layer delaminating and in some instances material detachment in the cathet 1170 catheters
2024-03-21 Class I Under Investigation by firm An increase in complaints related to an inability to advance the guidewire through the lumen of the device for certain batches. There is evidence of the polyurethane layer delaminating and in some instances material detachment in the cathet 5510 catheters
2024-03-21 Class I Under Investigation by firm An increase in complaints related to an inability to advance the guidewire through the lumen of the device for certain batches. There is evidence of the polyurethane layer delaminating and in some instances material detachment in the cathet 10 catheters
2024-03-21 Class I Under Investigation by firm An increase in complaints related to an inability to advance the guidewire through the lumen of the device for certain batches. There is evidence of the polyurethane layer delaminating and in some instances material detachment in the cathet 4715 catheters
2024-03-21 Class I Under Investigation by firm An increase in complaints related to an inability to advance the guidewire through the lumen of the device for certain batches. There is evidence of the polyurethane layer delaminating and in some instances material detachment in the cathet 2314 catheters
2024-03-21 Class I Under Investigation by firm An increase in complaints related to an inability to advance the guidewire through the lumen of the device for certain batches. There is evidence of the polyurethane layer delaminating and in some instances material detachment in the cathet 4942 catheters
2024-03-21 Class I Under Investigation by firm An increase in complaints related to an inability to advance the guidewire through the lumen of the device for certain batches. There is evidence of the polyurethane layer delaminating and in some instances material detachment in the cathet 4270 catheters
2024-03-21 Class I Under Investigation by firm An increase in complaints related to an inability to advance the guidewire through the lumen of the device for certain batches. There is evidence of the polyurethane layer delaminating and in some instances material detachment in the cathet 1950 catheters
2024-03-21 Class I Under Investigation by firm An increase in complaints related to an inability to advance the guidewire through the lumen of the device for certain batches. There is evidence of the polyurethane layer delaminating and in some instances material detachment in the cathet 25617 catheters
2024-03-21 Class I Under Investigation by firm An increase in complaints related to an inability to advance the guidewire through the lumen of the device for certain batches. There is evidence of the polyurethane layer delaminating and in some instances material detachment in the cathet 440 catheters
2024-03-21 Class I Under Investigation by firm An increase in complaints related to an inability to advance the guidewire through the lumen of the device for certain batches. There is evidence of the polyurethane layer delaminating and in some instances material detachment in the cathet 9271 catheters
2024-03-21 Class I Under Investigation by firm An increase in complaints related to an inability to advance the guidewire through the lumen of the device for certain batches. There is evidence of the polyurethane layer delaminating and in some instances material detachment in the cathet 8575 catheters
2024-03-21 Class I Under Investigation by firm An increase in complaints related to an inability to advance the guidewire through the lumen of the device for certain batches. There is evidence of the polyurethane layer delaminating and in some instances material detachment in the cathet 0
2024-03-21 Class I Under Investigation by firm An increase in complaints related to an inability to advance the guidewire through the lumen of the device for certain batches. There is evidence of the polyurethane layer delaminating and in some instances material detachment in the cathet 330 catheters

Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.

Where China Actually Supplies

Every device page names the company that lists it and the factories registered to make the same thing. These are the sections with the most of them.

5,100manufacturers registered in China
2,581device types they are registered for
340,248device records, each naming its maker
31provinces with a registered manufacturer