Identity
- Trade Name
- ASP GLOBAL FDA UDI
- Generic Name
- Intermittent electronic patient thermometer FDA UDI
- Device Name
- THERMOMETER, RECTAL DIGITAL, ASP RED, 20 SECOND READ FDA UDI
- Model / Reference
- TTASP-RECTAL FDA UDI
- Description
- THERMOMETER, RECTAL DIGITAL, ASP RED, 20 SECOND READ FDA UDI
Identifiers
- Primary DI / UDI-DI
- 10840216107622 FDA UDI
- FDA Product Code
- FLL FDA UDI
- GMDN Term
- Intermittent electronic patient thermometer FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 880.2910 FDA UDI
- Commercial Distribution
- Not in Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
No
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
No
FDA UDI
Asp Global by Asp Global, LLC — 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
- Asp Global, LLC
Sources (1)
- FDA UDI f386a49e-2abb-42bf-8648-d828cc9724b0 35 fields · synced May 30, 2026