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Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

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Cerus Corporation

Certificate G10 104609 0014

Rev. Rev. 00Issued
Valid until
Mar 4, 2030

Certificate G10 104609 0014 is a valid Quality management system issued to Cerus Corporation and registered in EUDAMED. Valid until March 4, 2030. View the full certificate record on MD Atlas.

Overview

Certificate number
G10 104609 0014
Certificate type
Quality management system
Certificate status
Issued
Applicable legislation
MDR [Regulation (EU) 2017/745 on medical devices]
Version
1
Certificate ID
0123G10 104609 0014Rev. 00

Validity

Issued
Mar 5, 2025
Valid from
Mar 5, 2025
Valid until
Mar 4, 2030

Notified body

Notified body
TÜV SÜD Product Service GmbH
Notified body SRN
0123
Notified body country
Germany

Covered devices

No specific devices are listed for this certificate.

Characteristics

Sterile
No
Human tissues
No
Animal tissues
No
In vitro diagnostics
No
Initial registration
Yes
New device
No
Discard allowed
No
SSCP enabled
Yes
Mechanism of scrutiny
Yes
Intended medical purpose
No
SPP applicable
No
Conditions applicable
No
MOS outside EUDAMED
—
QMS/MOS type
Class IIb only

History

No status changes or preceding certificates are recorded.

Scope coverage

Class IIb1

1 scope

  • Z120402 - GENERAL MEDICINE THERAPEUTIC TREATMENT INSTRUMENTS; The INTERCEPT Illuminator is intended only for use in the INTERCEPT Blood System pathogen inactivation process to deliver UVA light for the photochemical treatment of blood products.
    Class IIb

Documents

LanguagesEN

Manufacturer

Manufacturer
Cerus Corporation
Manufacturer SRN
US-MF-000000765
Manufacturer country
United States