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Touch Cmc 1

by Keri Medical SA 9 variants

Ref T-CTO109

Active European Union

CE MDR

Valid until

15 Feb 2028

CE MDR certificate

FDA recalls

Not applicable

No FDA record for this device

Documents

1 certificate

Certifier Intertek Medical Notified Body AB

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 Number28620157857-03 Date20 Mar 2026IssuedStatusActive expires 15 Feb 2028

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
TOUCH CMC1 Prosthesis
Model / Reference
T-CTO109
Primary DI / UDI-DI
07640181162420
Basic UDI-DI
764018116010AV
EMDN Code
P090404 Hand prostheses trapezio-metacarpal components
Device Class
Class III
EU market of registration
France

Manufacturer details

EUDAMED SRN
CH-MF-000021960
Authorised representative
Keri Medical France FR-AR-000009590

Other devices from Keri Medical SA

See all devices from Keri Medical SA →

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