Identity
- Trade Name
- Welch Allyn, Inc. FDA UDI
- Generic Name
- Mechanical external stethoscope FDA UDI
- Device Name
- Arden Stethoscope with Aluminum Double-Head Chestpiece (Adult Diaphragm and Low-Frequency Bell), Single Lumen Latex-Free Tubing; 32 in/81.3 cm; Red FDA UDI
- Model / Reference
- 901039 FDA UDI
- Description
- Arden Stethoscope with Aluminum Double-Head Chestpiece (Adult Diaphragm and Low-Frequency Bell), Single Lumen Latex-Free Tubing; 32 in/81.3 cm; Red FDA UDI
Identifiers
- Catalog Number
- ARDEN-S2RD FDA UDI
- Primary DI / UDI-DI
- 00732094096408 FDA UDI
- FDA Product Code
- LDE FDA UDI
- GMDN Term
- Mechanical external stethoscope FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 870.1875 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
No
FDA UDI
Category: Mechanical external stethoscope
Welch Allyn, Inc. by Welch Allyn, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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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 I | Pending data |
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Manufacturer
- Manufacturer
- Welch Allyn, Inc.
Sources (1)
- FDA UDI 47e45d78-011b-4bfe-b64b-61bd2d29c5fd 35 fields · synced Jun 6, 2026