Amplatz

TFE Coated Curved Amplatz Ultra Stiff Wire Guide - Catheter Exchange

Registry build 21.09.26
10manufacturers in China registered for this device type
128catalogue numbers in this listing
26510(k) clearances naming this product code
40recalls on this code

Who Else Makes It

Concentrated in Beijing (4), Jiangsu (3), Guangdong (2). One is registered as a contract manufacturer, able to build to a specification.

Chinese manufacturers registered for FDA product code DQX
Manufacturer City Province Registered as Device types
Mehow Innovative (Huizhou) Ltd. Huizhou Guangdong Contract manufacturer 11
Shanghai JPY ION-Tech Co., Ltd. Shanghai Shanghai Contract manufacturer 70
Suzhou Prosteri Medical Technology Co., Ltd. Suzhou Jiangsu Contract manufacturer 20
Sunny Medical Device (Shenzhen) Co., Ltd. Shenzhen Guangdong Contract manufacturer 11
Lepu Medical Technology (Beijing) Co., Ltd. Beijing Beijing Manufacturer 7
Beijing Target Medical Technologies Inc. Beijing Beijing Contract manufacturer 7
Suzhou Zenith Vascular Scitech Limited Suzhou Jiangsu Manufacturer 6
Beijing Bywave Sensing Medical Technology Co., Ltd. Beijing Beijing Manufacturer 2
Shanghai Achieva Medical Suzhou Co., Ltd. Suzhou Jiangsu Manufacturer 2
Deepintec Scientific Co., Ltd. Beijing Beijing Manufacturer 2

Record

Regulatory record for Amplatz
Listed by Cook Incorporated, United States
FDA product code DQX
Device type Wire, Guide, Catheter
Device class Class 2
Regulation 21 CFR 870.1330
Establishment Contract manufacturer, Contract steriliser, Specification developer, Complaint-file establishment, Manufacturer, Exporter
Premarket notification Exempt
Record published 2016-09-24
Record revised 2022-01-31 (version 4)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Label carries lot or batch number, expiry date, manufacturing date
Storage Special storage condition: Store in dark, dry, cool place.
Distribution end date 2022-01-28

Catalogue Numbers

Catalogue numbers for Amplatz
Catalogue number Size Status
G28779 In distribution
G04001 In distribution
G27032 In distribution
G03219 In distribution
G10169 In distribution
G03031 In distribution
G03330 In distribution
G03579 In distribution
G23639 In distribution
G12107 In distribution
G10648 In distribution
G03917 In distribution
G36212 In distribution
G03331 In distribution
G09954 In distribution
G05067 In distribution
G04113 In distribution
G12493 In distribution
G29444 In distribution
G23640 In distribution
G03584 In distribution
G03547 In distribution
G03373 In distribution
G10051 In distribution
G06016 In distribution
G20320 In distribution
G27036 In distribution
G03562 In distribution
G03441 In distribution
G04483 In distribution
G03041 In distribution
G03430 In distribution
G19854 In distribution
G09485 In distribution
G03539 In distribution
G04237 In distribution
G03334 In distribution
G03044 In distribution
G03875 In distribution
G03565 In distribution
G04047 In distribution
G11837 In distribution
G23643 In distribution
G11674 In distribution
G27038 In distribution
G11675 In distribution
G08280 In distribution
G07515 In distribution
G03460 In distribution
G12232 In distribution
G03290 In distribution
G23637 In distribution
G27888 In distribution
G03750 In distribution
G04421 In distribution
G11684 In distribution
G03216 In distribution
G09955 In distribution
G28781 In distribution
G03053 In distribution
G03564 In distribution
G23642 In distribution
G03138 In distribution
G04055 In distribution
G03095 In distribution
G09956 In distribution
G04080 In distribution
G03264 In distribution
G08255 In distribution
G10052 In distribution
G10168 In distribution
G27035 In distribution
G27034 In distribution
G28783 In distribution
G04003 In distribution
G03042 In distribution
G04048 In distribution
G06801 In distribution
G09960 In distribution
G06848 In distribution
G28751 In distribution
G23644 In distribution
G08680 In distribution
G27040 In distribution
G03203 In distribution
G04187 In distribution
G09957 In distribution
G05108 In distribution
G03279 In distribution
G23641 In distribution
G23638 In distribution
G03463 In distribution
G04933 In distribution
G03372 Withdrawn
G03527 Withdrawn
G03475 Withdrawn
G03047 Withdrawn
G03343 Withdrawn
G47703 Withdrawn
G03217 Withdrawn
G11685 Withdrawn
G04104 Withdrawn
G03073 Withdrawn
G03349 Withdrawn
G10056 Withdrawn
G04310 Withdrawn
G04007 Withdrawn
G03956 Withdrawn
G03067 Withdrawn
G03377 Withdrawn
G03523 Withdrawn
G03747 Withdrawn
G03304 Withdrawn
G04422 Withdrawn
G03473 Withdrawn
G10652 Withdrawn
G04167 Withdrawn
G03048 Withdrawn
G10548 Withdrawn
G03043 Withdrawn
G03540 Withdrawn
G03560 Withdrawn
G04149 Withdrawn
G10523 Withdrawn
G28753 Withdrawn
G06817 Withdrawn
G03327 Withdrawn
G11254 Withdrawn

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Arrow Teleflex Medical LLC 625
Cook Cook Incorporated 410
Guidewire Argon Medical Devices, Inc. 173
Medline Industries, Inc. Medline Industries, Inc. 151
Guidewire Galt Medical Corp. 144
InQwire® Merit Medical Systems, Inc. 120
Angiographic Guide Wire Medtronic, Inc. 94
Glidewire Terumo Corp. 83
Starter™ Guidewire Lake Region Medical Limited 82
INT,Falcon Guide Wire Shanghai Kindly Medical Instruments Co., Ltd. 72
GuideRight™ St. Jude Medical 69
INT, FirstWire Shanghai Kindly Medical Instruments Co., Ltd. 65

Showing 12 of 525. All products under Wire, Guide, Catheter

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K182985 2019-07-22
K181353 2019-02-15
K183467 2019-01-11
K180830 2018-12-20
K181351 2018-06-14
K171997 2018-03-30
K171912 2018-03-19
K171764 2018-03-09
K171445 2018-01-10
K171948 2018-01-05
K171897 2017-08-21
K150802 2015-05-28
K130766 2013-07-17
K123707 2013-02-28
K110163 2011-02-25
K110009 2011-02-02
K091385 2009-08-07
K081337 2008-08-08
K070410 2007-04-27
K042611 2004-11-12
K983771 1998-11-12
K920891 1992-12-21
K920824 1992-10-16
K901899 1990-09-27
K880722 1988-08-19
K781393 1978-10-30

Recalls Naming This Product

1 recall names this product by its own identifier, the UDI on its label.

Recalls naming the identifiers of Amplatz
Recalled by Identified by Initiated FDA class Root cause Reason Quantity
Cook Incorporated UDI-DI 2022-08-16 Class II Under Investigation by firm Cook Medical identified that devices from the affected device lots may have a complete breach of the chevron seal of the packaging. Therefore, the sterility of affected devices may be compromised. 204 OUS

Recalls

39 of these are Class II. Class II means a temporary or reversible health consequence. 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
2026-03-05 Class II Incorrect or no expiration date Products from the affected device lots were labeled with expiration dates that exceed the true shelf life. 49 units
2026-03-05 Class II Incorrect or no expiration date Products from the affected device lots were labeled with expiration dates that exceed the true shelf life. 15 units
2026-03-05 Class II Incorrect or no expiration date Products from the affected device lots were labeled with expiration dates that exceed the true shelf life. 75 units
2024-10-14 Class II Labeling Change Control Devices from the affected device lots have labels that state the incorrect expiration dates. 10 units
2024-10-08 Class II Labeling Change Control Affected device lots have labels that state the incorrect expiration dates. 5,953 US; 2,528 OUS
2024-10-08 Class II Labeling Change Control Affected device lots have labels that state the incorrect expiration dates. 2,005 US; 1,145 OUS
2022-08-16 Class II Under Investigation by firm Cook Medical identified that devices from the affected device lots may have a complete breach of the chevron seal of the packaging. Therefore, the sterility of affected devices may be compromised. 1,236 US
2022-08-16 Class II Under Investigation by firm Cook Medical identified that devices from the affected device lots may have a complete breach of the chevron seal of the packaging. Therefore, the sterility of affected devices may be compromised. 488 US, 5 OUS
2022-08-16 Class II Under Investigation by firm Cook Medical identified that devices from the affected device lots may have a complete breach of the chevron seal of the packaging. Therefore, the sterility of affected devices may be compromised.
2022-08-16 Class II Under Investigation by firm Cook Medical identified that devices from the affected device lots may have a complete breach of the chevron seal of the packaging. Therefore, the sterility of affected devices may be compromised. 9,903 US; 5,185 OUS
2022-08-16 Class II Under Investigation by firm Cook Medical identified that devices from the affected device lots may have a complete breach of the chevron seal of the packaging. Therefore, the sterility of affected devices may be compromised. 363 US; 244 OUS
2022-08-16 Class II Under Investigation by firm Cook Medical identified that devices from the affected device lots may have a complete breach of the chevron seal of the packaging. Therefore, the sterility of affected devices may be compromised. 2,748 US; 302 OUS
2022-08-16 Class II Under Investigation by firm Cook Medical identified that devices from the affected device lots may have a complete breach of the chevron seal of the packaging. Therefore, the sterility of affected devices may be compromised. No distribution (Distribution Center only)
2022-08-16 Class II Under Investigation by firm Cook Medical identified that devices from the affected device lots may have a complete breach of the chevron seal of the packaging. Therefore, the sterility of affected devices may be compromised. 43 OUS
2022-08-16 Class II Under Investigation by firm Cook Medical identified that devices from the affected device lots may have a complete breach of the chevron seal of the packaging. Therefore, the sterility of affected devices may be compromised. 5571 US, 409 OUS
2022-08-16 Class II Under Investigation by firm Cook Medical identified that devices from the affected device lots may have a complete breach of the chevron seal of the packaging. Therefore, the sterility of affected devices may be compromised. 202 US; 11 OUS
2022-08-16 Class II Under Investigation by firm Cook Medical identified that devices from the affected device lots may have a complete breach of the chevron seal of the packaging. Therefore, the sterility of affected devices may be compromised. 149 US
2022-08-16 Class II Under Investigation by firm Cook Medical identified that devices from the affected device lots may have a complete breach of the chevron seal of the packaging. Therefore, the sterility of affected devices may be compromised. 5041 US; 298 OUS
2022-08-16 Class II Under Investigation by firm Cook Medical identified that devices from the affected device lots may have a complete breach of the chevron seal of the packaging. Therefore, the sterility of affected devices may be compromised. 25 US
2022-08-16 Class II Under Investigation by firm Cook Medical identified that devices from the affected device lots may have a complete breach of the chevron seal of the packaging. Therefore, the sterility of affected devices may be compromised. No distribution (Distribution Center only)
2022-08-16 Class II Under Investigation by firm Cook Medical identified that devices from the affected device lots may have a complete breach of the chevron seal of the packaging. Therefore, the sterility of affected devices may be compromised. 58 US; 5 OUS
2022-08-16 Class II Under Investigation by firm Cook Medical identified that devices from the affected device lots may have a complete breach of the chevron seal of the packaging. Therefore, the sterility of affected devices may be compromised. 115 US
2022-08-16 Class II Under Investigation by firm Cook Medical identified that devices from the affected device lots may have a complete breach of the chevron seal of the packaging. Therefore, the sterility of affected devices may be compromised. 150 US, 97 OUS
2022-08-16 Class II Under Investigation by firm Cook Medical identified that devices from the affected device lots may have a complete breach of the chevron seal of the packaging. Therefore, the sterility of affected devices may be compromised. 5,669 US; 5,286 OUS
2022-08-16 Class II Under Investigation by firm Cook Medical identified that devices from the affected device lots may have a complete breach of the chevron seal of the packaging. Therefore, the sterility of affected devices may be compromised. 277 US; 138 OUS
2022-08-16 Class II Under Investigation by firm Cook Medical identified that devices from the affected device lots may have a complete breach of the chevron seal of the packaging. Therefore, the sterility of affected devices may be compromised. 42 US
2022-08-16 Class II Under Investigation by firm Cook Medical identified that devices from the affected device lots may have a complete breach of the chevron seal of the packaging. Therefore, the sterility of affected devices may be compromised. 1,501 US; 380 OUS
2022-07-19 Class II Under Investigation by firm Product did not meet the acceptance criteria for packaging testing, which included 3-year age acceleration testing, therefore, the sterility of the device may be compromised. 30 units
2022-07-19 Class II Under Investigation by firm Product did not meet the acceptance criteria for packaging testing, which included 3-year age acceleration testing, therefore, the sterility of the device may be compromised. 865 units
2022-07-19 Class II Under Investigation by firm Product did not meet the acceptance criteria for packaging testing, which included 3-year age acceleration testing, therefore, the sterility of the device may be compromised. 496 units
2022-07-19 Class II Under Investigation by firm Product did not meet the acceptance criteria for packaging testing, which included 3-year age acceleration testing, therefore, the sterility of the device may be compromised. 85 units
2022-07-19 Class II Under Investigation by firm Product did not meet the acceptance criteria for packaging testing, which included 3-year age acceleration testing, therefore, the sterility of the device may be compromised. 585 units
2022-07-19 Class II Under Investigation by firm Product did not meet the acceptance criteria for packaging testing, which included 3-year age acceleration testing, therefore, the sterility of the device may be compromised. 1450 units
2022-07-19 Class II Under Investigation by firm Product did not meet the acceptance criteria for packaging testing, which included 3-year age acceleration testing, therefore, the sterility of the device may be compromised. 15 units
2022-07-19 Class II Under Investigation by firm Product did not meet the acceptance criteria for packaging testing, which included 3-year age acceleration testing, therefore, the sterility of the device may be compromised. 35 units
2022-07-19 Class II Under Investigation by firm Product did not meet the acceptance criteria for packaging testing, which included 3-year age acceleration testing, therefore, the sterility of the device may be compromised. 189 units
2022-07-19 Class II Under Investigation by firm Product did not meet the acceptance criteria for packaging testing, which included 3-year age acceleration testing, therefore, the sterility of the device may be compromised. 5400 units
2022-07-19 Class II Under Investigation by firm Product did not meet the acceptance criteria for packaging testing, which included 3-year age acceleration testing, therefore, the sterility of the device may be compromised. 75 units
2022-07-19 Class II Under Investigation by firm Product did not meet the acceptance criteria for packaging testing, which included 3-year age acceleration testing, therefore, the sterility of the device may be compromised. 2407 units

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