Graftmaster

GRAFTMASTER Coronary Stent Graft System 4.50 mm x 26 mm / Rapid-Exchange

Registry build 21.09.26
1manufacturer
9catalogue numbers in this listing

Who Else Makes It

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

Chinese manufacturers registered for FDA product code DYG
Manufacturer City Province Registered as Device types
Bioxin Medical Co., Ltd. Weihai Shandong Contract manufacturer 8

Record

Regulatory record for Graftmaster
Listed by Abbott Vascular, United States
FDA product code DYG
Device type Catheter, Flow Directed
Device class Class 2
Regulation 21 CFR 870.1240
Establishment Specification developer, Complaint-file establishment, Manufacturer, Exporter
Record published 2014-11-21
Record revised 2019-10-07 (version 4)

Specifications

Specifications
MRI safety MR Conditional
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Label carries lot or batch number, expiry date
Storage Special storage condition: Store in a dry, dark, cool place

Catalogue Numbers

Catalogue numbers for Graftmaster
Catalogue number Size Status
1012583-26 In distribution
1012580-19 In distribution
1012580-26 In distribution
1012581-16 In distribution
1012582-19 In distribution
1012583-19 In distribution
1012584-19 In distribution
1012581-26 In distribution
1012581-19 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Arrow Teleflex Medical LLC 115
Transonic Transonic Systems, Inc. 12
Corodyn B. Braun Medical Inc. 10
Venos Occlusion Balloon Catheter Oscor Inc. 9
Swan-Ganz True Size Edwards Lifesciences Technology Sarl 9
Swan-Ganz Edwards Lifesciences Technology Sarl 7
Pruitt Occlusion Catheter Lemaitre Vascular, Inc. 6
Swan-Ganz VIP Edwards Lifesciences Technology Sarl 3
Swan-Ganz Becton, Dickinson AND Company 3
Swan Ganz Catheter Edwards Lifesciences Technology Sarl 2
Swan-Ganz Ccombo Edwards Lifesciences Technology Sarl 2
Cook Cook Incorporated 2

Showing 12 of 23. All products under Catheter, Flow Directed

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