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INTERCEPT Blood System for Plasma

FDA UDI

Class III (US FDA UDI)

by Cerus Corporation

Identity

Trade Name
INTERCEPT Blood System for Plasma FDA UDI
Generic Name
Donor blood photochemical treatment kit FDA UDI
Device Name
INTERCEPT Blood System for Plasma, Plasma (P) Processing Set FDA UDI
Model / Reference
INT3130B FDA UDI
Description
INTERCEPT Blood System for Plasma, Plasma (P) Processing Set FDA UDI

Identifiers

Primary DI / UDI-DI
18717953196993 FDA UDI
FDA Product Code
PJF FDA UDI
GMDN Term
Donor blood photochemical treatment kit 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

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: Donor blood photochemical treatment kit

INTERCEPT Blood System for Plasma by Cerus Corporation — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Donor blood photochemical treatment kit.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Cerus Corporation

Sources (1)

  • FDA UDI 059e5723-2302-42f1-b8d8-5f7ed8b7a4fd 34 fields · synced May 31, 2026