Identity
- Trade Name
- Thermasplint FDA UDI
- Generic Name
- Thermoplastic-moulding water bath FDA UDI
- Device Name
- Smith & Nephew 1501 w/ 220V U.K Cord(LG) FDA UDI
- Model / Reference
- SM-1501B-CORD2 FDA UDI
- Description
- Smith & Nephew 1501 w/ 220V U.K Cord(LG) FDA UDI
Identifiers
- Catalog Number
- SM1501BCORD2 FDA UDI
- Primary DI / UDI-DI
- 00645724003540 FDA UDI
- FDA Product Code
- IRQ FDA UDI
- GMDN Term
- Thermoplastic-moulding water bath FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 890.5950 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
No
FDA UDI
Over-the-Counter
Yes
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
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Thermoplastic-moulding water bath
Thermasplint by Whitehall Manufacturing Co — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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- Thermasplint — Whitehall Manufacturing Co · Class I
- Thermasplint — Whitehall Manufacturing Co · Class I
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
- Whitehall Manufacturing Co
Sources (1)
- FDA UDI d5f7c08b-b135-4672-b246-1106721629e5 34 fields · synced May 30, 2026