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3CP™ Centrifuge

FDA UDI

Class I (US FDA UDI)

by Reapplix ApS

Identity

Trade Name
3CP™ Centrifuge FDA UDI
Generic Name
Haematological concentrate system centrifuge FDA UDI
Device Name
This label goes directly on the centrifuge. The 3CP Centrifuge is a table-top centrifuge that creates the output (i.e., PRP). FDA UDI
Model / Reference
1 FDA UDI
Description
This label goes directly on the centrifuge. The 3CP Centrifuge is a table-top centrifuge that creates the output (i.e., PRP). FDA UDI

Identifiers

Primary DI / UDI-DI
05714188021577 FDA UDI
FDA Product Code
JQC FDA UDI
GMDN Term
Haematological concentrate system centrifuge FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
862.2050 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

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

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Haematological concentrate system centrifuge

3CP™ Centrifuge by Reapplix ApS — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Haematological concentrate system centrifuge.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Reapplix ApS

Sources (1)

  • FDA UDI 8f0babc5-e2f6-4d21-91f2-2b25421350c9 34 fields · synced May 31, 2026