Identity
- Trade Name
- CLINITUBES D941G-80-140X5 FDA UDI
- Generic Name
- Capillary blood collection tube IVD, sodium heparin FDA UDI
- Device Name
- D941G-80-140x5 CLINITUBES 5 vials of 50 units. 140 µL. Multipack w. accessories FDA UDI
- Model / Reference
- 942-882 FDA UDI
- Description
- D941G-80-140x5 CLINITUBES 5 vials of 50 units. 140 µL. Multipack w. accessories FDA UDI
Identifiers
- Catalog Number
- 942-882 FDA UDI
- Primary DI / UDI-DI
- 05700699428820 FDA UDI
- FDA Product Code
- GIO FDA UDI
- GMDN Term
- Capillary blood collection tube IVD, sodium heparin FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 864.6150 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
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
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Clinitubes D941g-80-140x5 by Radiometer Medical ApS — Class I — 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 I | Pending data |
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Manufacturer
- Manufacturer
- Radiometer Medical ApS
Sources (1)
- FDA UDI 708e638c-10e0-46a0-a1a7-361ee253dfc3 37 fields · synced Jun 8, 2026