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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
Aneroid manual sphygmomanometer FDA UDI
Device Name
GS777 WALL TRANSFORMER W 52400-PF AUS FDA UDI
Model / Reference
901027 FDA UDI
Description
GS777 WALL TRANSFORMER W 52400-PF AUS FDA UDI

Identifiers

Catalog Number
77516 FDA UDI
Primary DI / UDI-DI
00732094174021 FDA UDI
FDA Product Code
GCW FDA UDI
GMDN Term
Aneroid manual sphygmomanometer FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.1500 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

Yes

FDA UDI

Category: Aneroid manual sphygmomanometer

Welch Allyn, Inc. GS777 WALL TRANSFORMER W 52400-PF AUS is a comprehensive medical device designed to measure blood pressure with high accuracy and reliability. This aneroid manual sphygmomanometer features a portable design that allows for convenient use in various settings, including home or office environments. Its durable construction and user-friendly interface make it an ideal choice for healthcare professionals and patients alike.

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
Welch Allyn, Inc.

Sources (1)

  • FDA UDI aa31f5ed-0353-4eac-b770-b6e59b35e39b 35 fields · synced Jul 18, 2026