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Welch Allyn, Inc.

FDA UDI

Class II (US FDA UDI)

by Welch Allyn, Inc.

Identity

Trade Name
Welch Allyn, Inc. FDA UDI
Generic Name
Hearing aid enhanced audio device, teaching-environment FDA UDI
Device Name
WFR CSM NIBP WA Braun Pro6000 FDA UDI
Model / Reference
901058 FDA UDI
Description
WFR CSM NIBP WA Braun Pro6000 FDA UDI

Identifiers

Catalog Number
74WE FDA UDI
Primary DI / UDI-DI
00732094338775 FDA UDI
FDA Product Code
MWI FDA UDI
GMDN Term
Hearing aid enhanced audio device, teaching-environment FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.2300 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

Yes

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Hearing aid enhanced audio device, teaching-environment

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

Similar devices

Also classified as Hearing aid enhanced audio device, teaching-environment.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Welch Allyn, Inc.

Sources (1)

  • FDA UDI 8423b817-9c06-4a04-aac0-29f66e2e5f91 35 fields · synced Jun 1, 2026