Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3007170494

FEI Number

3007170494

Entity Name

Cerus Europe BV

City/State/Country

Amersfoort Utrecht, NL

Establishment Address

Stationsstraat 79-D, 3811 MH Amersfoort, Amersfoort Utrecht 3811 MH, NL

Establishment Type(s)

Export Device to the United States But Perform No Other Operation on Device,Repack or Relabel Medical Device

Owner / Operator

Cerus Corporation (Owner Number: 10048354)

Owner / Operator Contact Address

1220 Concord Ave, Concord, CA 94520, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

BP140143

All Registered Proprietary Names

INTERCEPT Processing Set for plasma INTERCEPT Processing Set for platelets INTERCEPT Blood System for Plasma INTERCEPT Blood System for Cryoprecipitation INTERCEPT Blood System for Platelets

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
PJF	Illuminator System For Blood Products	Unknown	Class 3	N/A	2017-12-07
PJF	Illuminator System For Blood Products	Unknown	Class 3	N/A	2015-01-02
PJF	Illuminator System For Blood Products	Unknown	Class 3	N/A	2015-01-02

Official Correspondent

Jennifer Yonemura

US Agent Details

Jennifer Yonemura Business: Cerus Corporation Email: jyonemura@cerus.com Phone: (925) 3483354

Related Public Records

Same Entity

Cerus Corporation

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

Other Registrations for Same Entity

Registration Number	Establishment Name	Location
3003925919	CERUS CORPORATION	Concord, CA, US

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9611902	Fenwal France S.A.S.	Lacs Indre, FR
3003925919	CERUS CORPORATION	Concord, CA, US
1058584	Sterigenics US LLC	Charlotte, NC, US
3031365458	WOMED SAS	Montpellier Herault, FR

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3007170494. Last updated year: 2026. Please use registration number 3007170494 when referencing this establishment in official correspondence.