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Welch Allyn, Inc.

FDA UDI

Class I (US FDA UDI)

by Welch Allyn, Inc.

Identity

Trade Name
Welch Allyn, Inc. FDA UDI
Generic Name
Basic power supply, reusable FDA UDI
Device Name
Welch Allyn 767 Mobile Aneroid Sphygmomanometer with Five-Leg Mobile Stand; Size-11 Adult, Reusable (Two Piece), 2-Tube Cuff; Premium Inflation Bulb and Valve, Coiled Tube (4.0 ft/1.2 m) FDA UDI
Model / Reference
901091 FDA UDI
Description
Welch Allyn 767 Mobile Aneroid Sphygmomanometer with Five-Leg Mobile Stand; Size-11 Adult, Reusable (Two Piece), 2-Tube Cuff; Premium Inflation Bulb and Valve, Coiled Tube (4.0 ft/1.2 m) FDA UDI

Identifiers

Catalog Number
7670-10CB FDA UDI
Primary DI / UDI-DI
00732094071399 FDA UDI
FDA Product Code
HMF FDA UDI
GMDN Term
Basic power supply, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
886.1860 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Basic power supply, reusable

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

Similar devices

Also classified as Basic power supply, reusable.

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 b8f671d3-d584-4426-9f77-2fb8661a7f62 35 fields · synced May 30, 2026