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BV Medical

FDA UDI

Class II (US FDA UDI)

by Medical, Inc.

Identity

Trade Name
BV Medical FDA UDI
Generic Name
Blood pressure cuff, reusable FDA UDI
Device Name
Sphygmomanometer Cuff & One-Tube Bladder, Black Nylon, Adult, Latex Free FDA UDI
Model / Reference
21-058-014 FDA UDI
Description
Sphygmomanometer Cuff & One-Tube Bladder, Black Nylon, Adult, Latex Free FDA UDI

Identifiers

Primary DI / UDI-DI
00845821002259 FDA UDI
FDA Product Code
DXQ FDA UDI
GMDN Term
Blood pressure cuff, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.1120 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

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Blood pressure cuff, reusable

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

Similar devices

Also classified as Blood pressure 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 240cadfc-0aa3-407f-9101-840623ea980e 34 fields · synced May 31, 2026