Vida®

FDA UDI

Class II (US FDA UDI)

by Bard Peripheral Vascular

Identity

Trade Name: VIDA® FDA UDI
Generic Name: Cardiac valvuloplasty catheter FDA UDI
Device Name: VIDA® BAV Balloon Valvuloplasty Catheter, 18mm x 4cm, 100cm catheter FDA UDI
Model / Reference: BAV184008 FDA UDI
Description: VIDA® BAV Balloon Valvuloplasty Catheter, 18mm x 4cm, 100cm catheter FDA UDI

Identifiers

Catalog Number: BAV184008 FDA UDI
Primary DI / UDI-DI: 00801741127854 FDA UDI
FDA Product Code: OZT FDA UDI
GMDN Term: Cardiac valvuloplasty catheter FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 870.1255 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

Category: Cardiac valvuloplasty catheter

Vida® by Bard Peripheral Vascular — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Bard Peripheral Vascular

Sources (1)

FDA UDI dbdeed03-60a3-4a04-ad3a-7019159bed15 36 fields · synced Jun 1, 2026