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Surelift Uplift

by Desarrollo E Investigacion Medica Aragonesa S.L. 4 variants

Ref UPLIFT04

Active European Union

CE MDR

Valid until

30 Aug 2031

CE MDR certificate

FDA recalls

Not applicable

No FDA record for this device

Documents

1 certificate

Certifier TÜV Rheinland LGA Products GmbH

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number843656835UPLIFTXB Basic UDI-DI 08437007606706UDI-DIDate18 Sep 2026RegisteredStatusActive

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)
  • IZ 1789390-6 Active Supplemented

    Technical documentation EU MDR

    Certifier
    TÜV Rheinland LGA Products GmbH 0197
    Issued
    8 Sep 2026
    Expires
    30 Aug 2031
    Reason
    Other

Coverage

1 jurisdiction

NetherlandsGermanyCzech RepublicPortugalSpainItaly
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDR Active

  • Czechia
  • Germany
  • Italy
  • Netherlands
  • Portugal
  • Spain

Specification

EUDAMED

Device Name
Surelift Uplift
Model / Reference
UPLIFT04
Primary DI / UDI-DI
08437007606706
Basic UDI-DI
843656835UPLIFTXB
EMDN Code
P0899 Urogenital prostheses - other
Device Class
Class III
EU market of registration
Spain

Manufacturer details

EUDAMED SRN
ES-MF-000004008

Other devices from Desarrollo E Investigacion Medica Aragonesa SL

See all devices from Desarrollo E Investigacion Medica Aragonesa SL →

Properties

  • Sterile
  • Implantable

Other properties (11)

  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No