Identity
- Trade Name
- CLINITUBES D956G-70-35*1 FDA UDI
- Generic Name
- Capillary blood collection tube IVD, electrolyte-balanced heparin FDA UDI
- Device Name
- D956G-70-35x1 CLINITUBES 1 vial of 75 units. 35 µL. Multipack w. accessories FDA UDI
- Model / Reference
- 905-661 FDA UDI
- Description
- D956G-70-35x1 CLINITUBES 1 vial of 75 units. 35 µL. Multipack w. accessories FDA UDI
Identifiers
- Catalog Number
- 905-661 FDA UDI
- Primary DI / UDI-DI
- 05700699056610 FDA UDI
- FDA Product Code
- GIO FDA UDI
- GMDN Term
- Capillary blood collection tube IVD, electrolyte-balanced 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 D956g-70-35*1 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 89eaeb2a-c3a1-4bc8-aafb-18ad91d2c347 36 fields · synced Jun 6, 2026