Identity
- Trade Name
- VACUETTE FDA UDI
- Generic Name
- Basic intravenous administration set, invasive FDA UDI
- Device Name
- VACUETTE® EVOPROTECT SAFETY Blood Collection Set + Luer Adapter 23G x 3/4" tubing length 12" (30 cm), single-packed, sterile, not made with natural rubber latex or DEHP FDA UDI
- Model / Reference
- 450130 FDA UDI
- Description
- VACUETTE® EVOPROTECT SAFETY Blood Collection Set + Luer Adapter 23G x 3/4" tubing length 12" (30 cm), single-packed, sterile, not made with natural rubber latex or DEHP FDA UDI
Identifiers
- Catalog Number
- 450130 FDA UDI
- Primary DI / UDI-DI
- 19120049206633 FDA UDI
- 510(k) Number
- K173757 FDA UDI
- FDA Product Code
- FMI FDA UDI
- GMDN Term
- Basic intravenous administration set, invasive FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 880.5570 FDA UDI
- Commercial Distribution
- 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
Category: Basic intravenous administration set, invasive
Vacuette by Greiner Bio-One GmbH — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Cleared under the same submission
K173757 also covers:
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 ff8c5b77-4e8d-40b7-b56f-4d916edfe34c 36 fields · synced May 31, 2026