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Gps® Iii Platelet Concentration System

FDA UDI

Class I (US FDA UDI)

by Biomet Biologics, LLC

Identity

Trade Name
GPS® III PLATELET CONCENTRATION SYSTEM FDA UDI
Generic Name
Haematological concentrate system FDA UDI
Model / Reference
800-1007A FDA UDI

Identifiers

Catalog Number
800-1007A FDA UDI
Primary DI / UDI-DI
00880304681514 FDA UDI
FDA Product Code
KSS FDA UDI
GMDN Term
Haematological concentrate system FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
864.9050 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Haematological concentrate system

Gps® Iii Platelet Concentration System by Biomet Biologics, LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Haematological concentrate system.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 2bb90f9b-fa03-471d-9d92-4c81b7b8db4d 36 fields · synced May 30, 2026