Percufix™ Catheter Cuff

Catheter Cuff

Registry build 21.09.26
9manufacturers in China registered for this device type
1catalogue number
5510(k) clearances naming this product code
2recalls on this code

Who Else Makes It

Concentrated in Jiangsu (3), Zhejiang (3), Guangdong (2). 6 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code KOD
Manufacturer City Province Registered as Device types
Well Lead Medical Co., Ltd. Guangzhou Guangdong Contract manufacturer 46
Suzhou Jingle Polymer Medical Apparatus Co., Ltd. Suzhou Jiangsu Contract manufacturer 19
Guangdong Ecan Medical Co., Ltd. Guangzhou Guangdong Contract manufacturer 14
Clinisupplies (Nanjing) Co., Ltd. Nanjing Jiangsu Contract manufacturer 13
Integral Medical Products Co., Ltd. Shaoxing Zhejiang Contract manufacturer 7
Hangzhou Jimushi Meditech Co., Ltd. Hangzhou Zhejiang Contract manufacturer 6
Sterigenics Shanghai ETO Ltd. Shanghai Shanghai Contract manufacturer 65
Steris Sterilization Technologies (Suzhou) Ltd Suzhou Jiangsu Contract manufacturer 44
Integral Sterilization Technology (Shaoxing) Co., Ltd. Shaoxing Zhejiang Contract manufacturer 5

Record

Regulatory record for Percufix™ Catheter Cuff
Listed by Boston Scientific Corporation, United States
FDA product code KOD
Device type Catheter, Urological
Device class Class 2
Regulation 21 CFR 876.5130
Establishment Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer, Exporter
Record published 2016-09-24
Record revised 2026-05-18 (version 7)

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
Packaging Pack of 10

Catalogue Numbers

Catalogue numbers for Percufix™ Catheter Cuff
Catalogue number Size Status
M001207000 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Rusch Teleflex Medical LLC 432
Dover Cardinal Health 200, LLC 163
Dover Cardinal Health 152
MTG HR Pharmaceuticals Inc. 59
Cook Cook Incorporated 43
Bardex® Lubricath® Foley Catheter C.R. Bard, Inc. 30
Magic3™ Intermittent Catheter C.R. Bard, Inc. 30
Ureteral Catheter Well Lead Medical Co., Ltd. 26
Bardex® Urethral Catheter Robinson Model C.R. Bard, Inc. 26
Personal Catheter™ Intermittent Catheter C.R. Bard, Inc. 24
DeRoyal Deroyal Industries, Inc. 23
Bard® Robinson Catheter C.R. Bard, Inc. 22

Showing 12 of 150. All products under Catheter, Urological

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K180530 2018-04-10
K102527 2010-11-05
K022135 2002-09-13
K011965 2001-07-13
K965229 1997-03-04

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
2012-03-15 Not classified Package design/selection Boston Scientific Corporation is initiating a Medical Device Recall of certain lots/batches of the Imager” II Catheter (Urology) and the Imager” II Angiographic Catheter. An investigation
has found that, during shipping, some units in the
11,340 (8,485 USA, 2,845 OUS) 2014-04-14
2009-10-22 Not classified Packaging process control The sterile barrier in the packaging (pouch) that contains the catheter may be breached. The breach of sterility could lead to a contamination of the device with subsequent transfer of infectious agents to the patient. 74 boxes (5/box) US; 18 boxes (5/box) OUS 2011-12-12

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