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BV Medical

FDA UDI

Class I (US FDA UDI)

by Medical, Inc.

Identity

Trade Name
BV Medical FDA UDI
Generic Name
Tourniquet cuff, reusable FDA UDI
Device Name
Velcro tourniquet, reusable, adult, latex free, royal blue, each FDA UDI
Model / Reference
80-806-254 FDA UDI
Description
Velcro tourniquet, reusable, adult, latex free, royal blue, each FDA UDI

Identifiers

Primary DI / UDI-DI
00845821027573 FDA UDI
FDA Product Code
GAX FDA UDI
GMDN Term
Tourniquet cuff, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.5900 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Tourniquet cuff, reusable

BV Medical by Medical, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Tourniquet cuff, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Medical, Inc.

Sources (1)

  • FDA UDI f8a7b223-6ea7-4741-a44c-d0b2af24c86c 34 fields · synced May 31, 2026