Cook

Removable Brush Biopsy Set Middle Calyces

Registry build 21.09.26
9manufacturers in China registered for this device type
43catalogue numbers in this listing
5510(k) clearances naming this product code
1recall

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 Cook
Listed by Cook Incorporated, United States
FDA product code KOD
Device type Catheter, Urological
Device class Class 2
Regulation 21 CFR 876.5130
Establishment Contract manufacturer, Contract steriliser, Specification developer, Complaint-file establishment, Manufacturer, Exporter
Record published 2016-09-24
Record revised 2019-08-22 (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.
Packaging Pack of 10
Distribution end date 2018-01-25

Catalogue Numbers

Catalogue numbers for Cook
Catalogue number Size Status
G14042 In distribution
G14941 In distribution
G17077 In distribution
G14238 In distribution
G14179 In distribution
G15885 In distribution
G15045 In distribution
G14818 In distribution
G14036 In distribution
G14274 In distribution
G14031 In distribution
G15112 In distribution
G14050 In distribution
G15803 In distribution
G14028 In distribution
G15113 In distribution
G14038 In distribution
G14092 In distribution
G14093 In distribution
G14415 In distribution
G14039 In distribution
G14045 In distribution
G15945 In distribution
G14873 In distribution
G14052 In distribution
G14430 In distribution
G14029 In distribution
G15500 In distribution
G14043 In distribution
G14456 In distribution
G14178 In distribution
G14090 In distribution
G14044 In distribution
G14429 In distribution
G14091 In distribution
G14037 In distribution
G16193 In distribution
G17078 In distribution
G17076 In distribution
G14030 In distribution
G14051 In distribution
G14919 In distribution
G15243 Withdrawn

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
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
Flexi-Tip Cook Incorporated 20

Showing 12 of 150. All products under Catheter, Urological

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K181144 2018-06-28
K171810 2018-03-07
K171600 2018-02-16
K171662 2018-02-01
K760858 1976-12-06

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
2010-12-13 Not classified Packaging process control The firm received a complaint that 15 units of the Koyle Diaper Stent were received in packages that had not been sealed. Each stent should be sealed in a poly-Tyvek pouch. 25 stents 2011-01-31

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