INTERCEPT Blood System for Cryoprecipitation

FDA UDI

Class III (US FDA UDI)

by Cerus Corporation

Identity

Trade Name: INTERCEPT Blood System for Cryoprecipitation FDA UDI
Generic Name: Blood washing/centrifugation bag FDA UDI
Device Name: INTERCEPT Blood System for Cryoprecipitation FDA UDI
Model / Reference: INT3230 FDA UDI
Description: INTERCEPT Blood System for Cryoprecipitation FDA UDI

Identifiers

Primary DI / UDI-DI: 18717953197013 FDA UDI
FDA Product Code: PJF FDA UDI
GMDN Term: Blood washing/centrifugation bag FDA UDI

Classification

Device Class: Class III FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

Yes

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

Category: Blood washing/centrifugation bag

INTERCEPT Blood System for Cryoprecipitation by Cerus Corporation — Class III — 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 III	Pending data

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Manufacturer

Manufacturer: Cerus Corporation

Sources (1)

FDA UDI 75cf47e3-e85e-40f1-acf8-92a5613ff82f 35 fields · synced May 30, 2026