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Baum

FDA UDI

Class II (US FDA UDI)

by W.a. Baum Co., Inc.

Identity

Trade Name
BAUM FDA UDI
Generic Name
Aneroid manual sphygmomanometer FDA UDI
Device Name
Test Kit - Y Connector With Non-Latex Bulb and Valve FDA UDI
Model / Reference
2941NL FDA UDI
Description
Test Kit - Y Connector With Non-Latex Bulb and Valve FDA UDI

Identifiers

Catalog Number
2941NL FDA UDI
Primary DI / UDI-DI
00810010923288 FDA UDI
FDA Product Code
DXQ FDA UDI
GMDN Term
Aneroid manual sphygmomanometer 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

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: Aneroid manual sphygmomanometer

Baum by W.a. Baum Co., Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Aneroid manual sphygmomanometer.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
W.a. Baum Co., Inc.

Sources (1)

  • FDA UDI d9a7da5c-8887-4953-ba57-fe6afa17f4ab 35 fields · synced Jun 1, 2026