Vida®

VIDA® BAV Balloon Valvuloplasty Catheter, 26mm x 4cm, 100cm catheter

Registry build 21.09.26
1manufacturer
5catalogue numbers in this listing
1510(k) clearance

Who Else Makes It

Registered in Guangdong.

Chinese manufacturers registered for FDA product code OZT
Manufacturer City Province Registered as Device types
Dongguan TT Medical, Inc. Dongguan Guangdong Manufacturer 4

Record

Regulatory record for Vida®
Listed by Bard Peripheral Vascular, Inc., United States
FDA product code OZT
Device type Balloon Aortic Valvuloplasty
Device class Class 2
Regulation 21 CFR 870.1255
Establishment Specification developer, Complaint-file establishment, Manufacturer
Record published 2016-09-16
Record revised 2018-03-29 (version 2)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Latex Labelled latex-free
Label carries lot or batch number, expiry date

Catalogue Numbers

Catalogue numbers for Vida®
Catalogue number Size Status
BAV264012 Balloon Length, 4 Centimeters In distribution
BAV184008 Shaft Length, 100 Centimeters In distribution
BAV224010 Balloon Length, 4 Centimeters In distribution
BAV244010 Shaft Length, 100 Centimeters In distribution
BAV204009 Shaft Length, 100 Centimeters In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Z-MED™ B. Braun Interventional Systems, Inc. 60
Z-MED II™ B. Braun Interventional Systems, Inc. 33
True Dilatation Bard Peripheral Vascular, Inc. 18
Inoue Balloon A Toray Industries, Inc. 12
V8 Intervalve, Inc. 12
KardiaPSI Intervention Tech, Inc. ; dba Corvention 11
NuCLEUS-X™ B. Braun Interventional Systems, Inc. 9
ValvuloPro® Dongguan TT Medical, Inc. 6
True Flow Bard Peripheral Vascular, Inc. 5
OutFlo Aortic Valve Valvuloplasty Dilatation Balloon Catheter Disa Medinotec (PTY) Ltd 5
Edwards Balloon Catheter Edwards Lifesciences Technology Sarl 1
Ascendra Balloon Aortic Valvuloplasty Catheter Edwards Lifesciences Technology Sarl 1

Showing 12 of 15. All products under Balloon Aortic Valvuloplasty

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K133569 2013-12-20

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