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Cerus Endovascular, Ltd.

Active in EUDAMED

United Kingdomfrom SRN EUDAMED FDA SRN GB-MF-000008548

Part of Cerus Endovascular, Inc.

Devices
10
Registrations
EUDAMEDFDA
FDA recalls
0

At a glance

Counted by deviCERTS from registry records

EU certificates

2 of 2 in force.

See certificates

Market reach

European Union
EUDAMED actor, 2 certificates
United States
FDA establishment

Catalogue10

Newest first, rows 1-10 of 10

  • Contour 021 Ref CNS21009-15

    Class III
    Active CE MDR EUDAMED III

  • Neqstent 021 Ref NQS21409-15

    Class III
    Active CE MDR EUDAMED III

  • Neqstent Ref NQS414-15

    Class III
    Active CE MDR EUDAMED III

  • Contour 021 Ref CNS21005-15

    Class III
    Active CE MDR EUDAMED III

  • Neqstent 021 Ref NQS21407-15

    Class III
    Active CE MDR EUDAMED III

  • Contour Neurovascular System Ref CNS011-15

    Class III
    Active CE MDR EUDAMED III

  • Cable Set Ref CAB701-01

    Class I
    Active CE MDR EUDAMED I

  • Neqstent 021 Ref NQS21411-15

    Class III
    Active CE MDR EUDAMED III

  • Contour Neurovascular System Ref CNS014-15

    Class III
    Active CE MDR EUDAMED III

  • Contour 021 Ref CNS21007-15

    Class III
    Active CE MDR EUDAMED III

Company details

EUDAMED SRN
GB-MF-000008548
EU VAT number
159 5773 59
EUDAMED status
Active since 2023
EUDAMED registered name
Cerus Endovascular, Ltd.
EUDAMED abbreviated name
Cerus Endovascular
Registered address
John Eccles House, OX4 4GP, Oxford, United Kingdom (ex Northern Ireland)
Phone
+1 510 413 2500
PRRC contact
Breskella Halteh(public in EUDAMED)

EUDAMED certificates2

2 certificates2 valid, 0 expiredMDR 2next expiry 20 Jun 2029

EUDAMED certificates (2)

Notified body 0297 2 certificates

  • 1000307201 Supplemented

    Technical documentation EU MDR

    Issued
    13 Apr 2026
    Expires
    20 Jun 2029
    Reason
    Change approved
  • 1000307203 Supplemented

    Quality management system EU MDR

    Issued
    13 Apr 2026
    Expires
    20 Jun 2029
    Reason
    Change approved

FDA establishments1

Registered with the FDA under this company group, matched by name.

  • Cerus Endovascular, Inc. Fremont, CA · US FEI 3013408612

Frequently asked questions

How many devices does Cerus Endovascular, Ltd. have in the registry?

The registry currently lists 10 devices for Cerus Endovascular, Ltd.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Cerus Endovascular, Ltd.'s devices?

Among its 10 most recently registered devices, Cerus Endovascular, Ltd. has devices listed in EUDAMED (10 devices).

What risk classes do Cerus Endovascular, Ltd.'s devices fall under?

Among its 10 most recently registered devices, the classes recorded for Cerus Endovascular, Ltd.'s devices are Class I and Class III. Each device page shows its own class and authorisation.

What EUDAMED certificates are recorded for Cerus Endovascular, Ltd.?

EUDAMED lists 2 certificates for Cerus Endovascular, Ltd. (technical documentation; quality management system) under MDR. The most recent was issued on 2026-04-13.

What are the newest devices from Cerus Endovascular, Ltd. in the registry?

The most recently registered devices listed for Cerus Endovascular, Ltd. include Contour 021, Neqstent 021, Neqstent and Contour Neurovascular System.

Which FDA establishments are linked to Cerus Endovascular, Ltd.?

1 FDA establishment is linked to Cerus Endovascular, Ltd. in the registry; they are listed on the company page.

Generated automatically from registry data and not verified by a human reviewer.