Identity
- Trade Name
- BIOS Diagnostics FDA UDI
- Generic Name
- Capillary patient thermometer, gallium-alloy FDA UDI
- Device Name
- Glass Thermometer FDA UDI
- Model / Reference
- 220DI FDA UDI
- Description
- Glass Thermometer FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00057475220495 FDA UDI
- FDA Product Code
- FLK FDA UDI
- GMDN Term
- Capillary patient thermometer, gallium-alloy FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 880.2920 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
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: Capillary patient thermometer, gallium-alloy
BIOS Diagnostics by Thermor Ltd — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Capillary patient thermometer, gallium-alloy.
- Geratherm® classic — Geratherm Medical AG · Class II
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
- Thermor Ltd
Sources (1)
- FDA UDI 1ff08163-9f95-4741-b117-82a7f8a2b606 33 fields · synced May 30, 2026