Identity
- Trade Name
- Vacuette FDA UDI
- Generic Name
- Non-fixed blood collection needle FDA UDI
- Device Name
- VACUETTE® Multiple Use Drawing Needle 22G x 1 1/2" black, sterile, not made with natural rubber latex 0.7 x 38 mm FDA UDI
- Model / Reference
- 450075 FDA UDI
- Description
- VACUETTE® Multiple Use Drawing Needle 22G x 1 1/2" black, sterile, not made with natural rubber latex 0.7 x 38 mm FDA UDI
Identifiers
- Catalog Number
- 450075 FDA UDI
- Primary DI / UDI-DI
- 29120017570206 FDA UDI
- 510(k) Number
- K973620 FDA UDI
- FDA Product Code
- FMI FDA UDI
- GMDN Term
- Non-fixed blood collection needle FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 880.5570 FDA UDI
- Commercial Distribution
- Not in Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
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
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Vacuette by Greiner Bio-One GmbH — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Cleared under the same submission
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
- Greiner Bio-One GmbH
Sources (1)
- FDA UDI dc803a67-dcc6-4e70-b692-8d0bc5573f64 37 fields · synced Jun 1, 2026