Vivaspin 6

FDA UDI

Class I (US FDA UDI)

by Sartorius Stedim Lab Limited

Identity

Trade Name: Vivaspin 6 FDA UDI
Generic Name: Centrifuge tube IVD FDA UDI
Device Name: This single-use device can be used for In Vitro Diagnostic applications, it is suitable for use to concentrate or separate serum, urine, and other bodily fluids prior to further sample analysis. FDA UDI
Model / Reference: VS0602IVD FDA UDI
Description: This single-use device can be used for In Vitro Diagnostic applications, it is suitable for use to concentrate or separate serum, urine, and other bodily fluids prior to further sample analysis. FDA UDI

Identifiers

Primary DI / UDI-DI: 05060602430044 FDA UDI
FDA Product Code: JJH FDA UDI
GMDN Term: Centrifuge tube IVD FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 862.2310 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

Category: Centrifuge tube IVD

Vivaspin 6 by Sartorius Stedim Lab Limited — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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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

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Manufacturer

Manufacturer: Sartorius Stedim Lab Limited

Sources (1)

FDA UDI 5a117d7c-ec78-4c22-876c-4d142688bfbb 35 fields · synced May 30, 2026