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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
Evacuated urine specimen container IVD, no additive FDA UDI
Device Name
VACUETTE® TUBE 9 ml Z Urine No Additive 16x100 yellow cap-yellow ring, Conical Base, non-ridged FDA UDI
Model / Reference
455028 FDA UDI
Description
VACUETTE® TUBE 9 ml Z Urine No Additive 16x100 yellow cap-yellow ring, Conical Base, non-ridged FDA UDI

Identifiers

Catalog Number
455028 FDA UDI
Primary DI / UDI-DI
29120017570916 FDA UDI
FDA Product Code
FMH FDA UDI
GMDN Term
Evacuated urine specimen container IVD, no additive 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

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: Evacuated urine specimen container IVD, no additive

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

Similar devices

Also classified as Evacuated urine specimen container IVD, no additive.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI d23da551-ff32-4d52-878e-ac5839079e47 35 fields · synced May 31, 2026