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Vacuette

FDA UDI

Class I (US FDA UDI)

by Greiner Bio-One GmbH

Identity

Trade Name
Vacuette FDA UDI
Generic Name
General tissue specimen container IVD, fixative/saline FDA UDI
Device Name
VACUETTE® 3 ml Virus Stabilization Tube 13x100 red cap-white ring, PREMIUM, USA FDA UDI
Model / Reference
456164 FDA UDI
Description
VACUETTE® 3 ml Virus Stabilization Tube 13x100 red cap-white ring, PREMIUM, USA FDA UDI

Identifiers

Catalog Number
456164 FDA UDI
Primary DI / UDI-DI
29120049208658 FDA UDI
FDA Product Code
JSG FDA UDI
GMDN Term
General tissue specimen container IVD, fixative/saline FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
866.2300 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: General tissue specimen container IVD, fixative/saline

Vacuette by Greiner Bio-One GmbH — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as General tissue specimen container IVD, fixative/saline.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 827f8a41-565f-4ab0-a79a-e85eb61f2aad 35 fields · synced May 31, 2026