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
Single Use
No
Implantable
No
Contains Latex
No
Prescription Use
Yes
Over-the-Counter
No
Convenience Kit
No
Combination Product
No
HCT/P
No
Premarket Exempt
No
Lot / Batch Number
Yes
Serial Number
No
Expiration Date
No
Manufacturing Date
Yes
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.
- Diagnostix™ — American Diagnostic Corporation · Class II
- Diagnostix™ — American Diagnostic Corporation · Class II
- e-mega® black, disinfectable one-piece cuff, small adult size 2-tube — Rudolf Riester GmbH & Co. KG · Class II
- Diagnostix™ — American Diagnostic Corporation · Class II
- Princess — American Diagnostic Corporation · Class II
- Diagnostix™ — American Diagnostic Corporation · Class II
- E-sphyg™ — American Diagnostic Corporation · Class II
- BAUM — W.A. BAUM CO., INC. · Class II
Authorization Coverage (1 country)
Regulatory Authorizations
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Welch Allyn, Inc.
Sources (1)
- FDA UDI aa31f5ed-0353-4eac-b770-b6e59b35e39b 35 fields · synced Jul 18, 2026