Identity
- Trade Name
- Welch Allyn, Inc. FDA UDI
- Generic Name
- Blood pressure cuff, reusable FDA UDI
- Device Name
- Welch Allyn Trimline Blood Pressure Cuff; Size-09 Child, Reusable, 2-Tubes (10.0 in/25.4 cm), Female Luer-Slip (#1391) Connectors FDA UDI
- Model / Reference
- 901043 FDA UDI
- Description
- Welch Allyn Trimline Blood Pressure Cuff; Size-09 Child, Reusable, 2-Tubes (10.0 in/25.4 cm), Female Luer-Slip (#1391) Connectors FDA UDI
Identifiers
- Catalog Number
- 1955F FDA UDI
- Primary DI / UDI-DI
- 00732094015409 FDA UDI
- FDA Product Code
- DXQ FDA UDI
- GMDN Term
- Blood pressure cuff, reusable FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 870.1120 FDA UDI
- Commercial Distribution
- Not 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
No
FDA UDI
Welch Allyn, Inc. by Welch Allyn, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
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Manufacturer
- Manufacturer
- Welch Allyn, Inc.
Sources (1)
- FDA UDI 0f8ab76d-8f2d-40de-b4a5-1b29d93e909d 36 fields · synced Jun 6, 2026