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Cellpreserv Kolplast

FDA UDI

Class I (US FDA UDI)

by Kolplast CI SA

Identity

Trade Name
CELLPRESERV KOLPLAST FDA UDI
Generic Name
Cytological centrifuge IVD FDA UDI
Model / Reference
CELLPRESERV CYTOCENTRIFUGE FDA UDI

Identifiers

Catalog Number
10.1315 FDA UDI
Primary DI / UDI-DI
07898027907630 FDA UDI
FDA Product Code
IFB FDA UDI
GMDN Term
Cytological centrifuge IVD FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
864.3300 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Cytological centrifuge IVD

Cellpreserv Kolplast by Kolplast CI SA — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Cytological centrifuge IVD.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Kolplast CI SA

Sources (1)

  • FDA UDI 2f88845a-8351-4ab4-a22e-01f5aaf70686 33 fields · synced Jun 8, 2026