Skip to content

Creo Medical

by Creo Medical, S.L.U. 40 variants

Ref 10017130BModel ScopeTrap

Active European Union

CE MDR

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None, self-declared

Class I: no certifier involved

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number843603713GT.0432S Basic UDI-DI 08436037137617UDI-DIDate7 Oct 2024RegisteredStatusActive

Certificates

0 certificates · EUDAMED

No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
Polytrap
Model / Reference
ScopeTrap, 10017130B
Primary DI / UDI-DI
08436037137617
Basic UDI-DI
843603713GT.0432S
Direct Marketing DI
08436037137617
EMDN Code
G03050199 Digestive endoscopy, retrieval devices - other
Device Class
Class I
EU market of registration
France

Manufacturer details

EUDAMED SRN
ES-MF-000000385

Other devices from Creo Medical, S.L.U.

See all devices from Creo Medical, S.L.U. →

Properties

Other properties (13)

  • Sterile: No
  • Implantable: No
  • 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