Wire, Guide, Catheter

5.5F (1.9MM ID) X 10CM Tearaway Introducer SET W/Nitinol Guidewire W/Radiopaque TIP

Registry build 21.09.26
10manufacturers in China registered for this device type
25catalogue numbers in this listing
1recall

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 Wire, Guide, Catheter
Listed by Medical Components Inc, United States
FDA product code DQX
Device type Wire, Guide, Catheter
Device class Class 2
Regulation 21 CFR 870.1330
Establishment Contract manufacturer, Reprocessor, Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer, Exporter
Record published 2019-07-03
Record revised 2021-12-22 (version 3)

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
Latex Labelled latex-free
Label carries lot or batch number, expiry date
Packaging Box of 5, box of 4, box of 20, box of 40, inner box of 10, box
Distribution end date 2024-10-17

Catalogue Numbers

Catalogue numbers for Wire, Guide, Catheter
Catalogue number Size Status
DMR190060 In distribution
TRAY #500 Withdrawn
MCK10 Withdrawn
TRAY #4C Withdrawn
MR195150 Withdrawn
TRAY #96 Withdrawn
TRAY #102A Withdrawn
MR190510 Withdrawn
TRAY #293 Withdrawn
TRAY #52 Withdrawn
TRAY #201 Withdrawn
TRAY #663 Withdrawn
TRAY #119 Withdrawn
DMR195535 Withdrawn
TRAY #328B Withdrawn
DMR190735 Withdrawn
MCT 100 Withdrawn
MC181A Withdrawn
MR190735 Withdrawn
TRAY #273 Withdrawn
DMRI19100801 Withdrawn
TRAY #277 Withdrawn
TRAY #322 Withdrawn
TRAY #45 Withdrawn
MR195535 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
Amplatz Cook Incorporated 128
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

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

Recalls

The FDA has not published a severity grade for these. 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 Closed
2008-04-11 Not classified Mixed-up of materials/components kit contains incorrect component 100 units 2008-10-28

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