Identity
- Trade Name
- COMBI *M sensor 82 FDA UDI
- Generic Name
- Transcutaneous blood gas monitor sensor FDA UDI
- Device Name
- COMBI *M sensor 82 FDA UDI
- Model / Reference
- 0605000 FDA UDI
- Description
- COMBI *M sensor 82 FDA UDI
Identifiers
- Catalog Number
- 0605000 FDA UDI
- Primary DI / UDI-DI
- 05700693095189 FDA UDI
- FDA Product Code
- KLK FDA UDILKD FDA UDI
- GMDN Term
- Transcutaneous blood gas monitor sensor FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 868.2500 FDA UDI868.2480 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
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
COMBI *M sensor 82 by Radiometer Basel AG — 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
- Radiometer Basel AG
Sources (1)
- FDA UDI c77f0260-8f32-4539-9ef9-ef122a55db88 37 fields · synced May 30, 2026