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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
Non-evacuated erythrocyte sedimentation rate (ESR) tube IVD FDA UDI
Device Name
ESR pipette with adapter, graduated 200 mm for 454073 FDA UDI
Model / Reference
727111 FDA UDI
Description
ESR pipette with adapter, graduated 200 mm for 454073 FDA UDI

Identifiers

Catalog Number
727111 FDA UDI
Primary DI / UDI-DI
29120017578158 FDA UDI
FDA Product Code
JPH FDA UDI
GMDN Term
Non-evacuated erythrocyte sedimentation rate (ESR) tube IVD FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
864.6700 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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Non-evacuated erythrocyte sedimentation rate (ESR) tube IVD

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

Similar devices

Also classified as Non-evacuated erythrocyte sedimentation rate (ESR) tube IVD.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Greiner Bio-One GmbH

Sources (1)

  • FDA UDI 97124bab-bb97-4ff9-971e-5eb65dcc4fd0 35 fields · synced Jun 8, 2026