Identity
- Trade Name
- Vacuette FDA UDI
- Generic Name
- General laboratory container, single-use FDA UDI
- Device Name
- VACUETTE® SECONDARY Tube MULTIPLEX PP 13x75 mm with orange screw closure, PREMIUM FDA UDI
- Model / Reference
- 459001 FDA UDI
- Description
- VACUETTE® SECONDARY Tube MULTIPLEX PP 13x75 mm with orange screw closure, PREMIUM FDA UDI
Identifiers
- Catalog Number
- 459001 FDA UDI
- Primary DI / UDI-DI
- 29120017578356 FDA UDI
- FDA Product Code
- NNI FDA UDI
- GMDN Term
- General laboratory container, single-use FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 864.3250 FDA UDI
- Commercial Distribution
- 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
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: General laboratory container, single-use
Vacuette by Greiner Bio-One GmbH — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as General laboratory container, single-use.
- CARDINAL HEALTH — Cardinal Health 200, LLC · Class I
- Micro-OSMETTE Sample Tubes, 50 ul — PRECISION SYSTEMS, INC. · Class I
- Marketlab — MARKETLAB INC. · Class I
- CARDINAL HEALTH — Cardinal Health 200, LLC · Class I
- Vial Set — Argon Medical Devices, Inc. · Class I
- KBMED — KB Medical (group), Inc. · Class I
- Gongdong — Zhejiang Gongdong Medical Technology Co., Ltd., · Class I
- Gongdong — Zhejiang Gongdong Medical Technology Co., Ltd., · Class I
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
- Greiner Bio-One GmbH
Sources (1)
- FDA UDI 66378488-bd29-4dd2-bad7-1d48621e3a43 35 fields · synced May 30, 2026