Identity
- Trade Name
- CLINITUBES D941G-NA-240-85X10 FDA UDI
- Generic Name
- Capillary blood collection tube IVD, sodium heparin FDA UDI
- Device Name
- D941G-NA-240-85x10 CLINITUBES 10 vials of 75 units, Multipack FDA UDI
- Model / Reference
- 942-876 FDA UDI
- Description
- D941G-NA-240-85x10 CLINITUBES 10 vials of 75 units, Multipack FDA UDI
Identifiers
- Catalog Number
- 942-876 FDA UDI
- Primary DI / UDI-DI
- 05700699428769 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-Na-240-85x10 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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Radiometer Medical ApS
Sources (1)
- FDA UDI 3352670a-3df1-44e9-b359-19072051e2cf 37 fields · synced May 30, 2026