CERUS CORPORATION

FDA Device Registration & Listing · Concord, CA, US · Registration 3003925919

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3003925919
FEI Number
3003925919
Entity Name
CERUS CORPORATION
City/State/Country
Concord, CA, US
Establishment Address
1220 Concord Ave, Concord, CA 94520, US
Establishment Type(s)
Complaint File Establishment per 21 CFR 820.198,Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
Cerus Corporation (Owner Number: 10048354)
Owner / Operator Contact Address
1220 Concord Ave, Concord, CA 94520, US
Initial Importer Flag
N
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 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

Official Correspondent

Jennifer Yonemura

US Agent Details

No US Agent registered (Local establishment).

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
3007170494 Cerus Europe BV Amersfoort Utrecht, NL

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3003925919. Last updated year: 2026. Please use registration number 3003925919 when referencing this establishment in official correspondence.
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