Petelin

Petelin Endoscopic Cholangiography Set

Registry build 21.09.26
1manufacturer
1catalogue number
1recall

Who Else Makes It

Registered in Zhejiang. One is registered as a contract manufacturer, able to build to a specification.

Chinese manufacturers registered for FDA product code GBZ
Manufacturer City Province Registered as Device types
Beilun Plastech Inc Ningbo Zhejiang Contract manufacturer 13

Record

Regulatory record for Petelin
Listed by Cook Incorporated, United States
FDA product code GBZ
Device type Catheter, Cholangiography
Device class Class 1
Regulation 21 CFR 878.4200
Establishment Contract manufacturer, Contract steriliser, Specification developer, Complaint-file establishment, Manufacturer, Exporter
Premarket notification Exempt
Record published 2020-10-02
Record revised 2020-11-19 (version 2)

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.

Catalogue Numbers

Catalogue numbers for Petelin
Catalogue number Size Status
G10664 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Taut Teleflex Medical LLC 31
PVC Thoracic Catheters Atrium Medical Corporation 30
Cook Cook Incorporated 12
Reddick Scoop Tip Cholangiogram Catheter Lemaitre Vascular, Inc. 8
Symmetry Surgical Aspen Surgical Products, Inc. 8
PMI Progressive Medical Technology, Inc. 8
Reddick Cholangiogram Catheter Lemaitre Vascular, Inc. 7
Olsen Cook Incorporated 7
Princeton Princeton Medical Group, Inc. 3
RX Ercp Cannula Boston Scientific Corporation 2
Metal Catheter RZ Medizintechnik Gmbh 2
Catheter, Cholangiography Edwards Lifesciences Technology Sarl 2

Showing 12 of 32. All products under Catheter, Cholangiography

Recalls

1 of these is 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 Closed
2015-05-28 Class II Component change control Cook Inc. is initiating a voluntary recall of the Ring Transjugular Intrahepatic Access Set and the Flexor RTPS Introduce Sheath due to complaints of the dilators being too long. 661 2017-05-30

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