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K650 Supporto anca

by Contel S.r.l. 9 variants

Ref K650 Supporto anca sinistra TG XL, SK445 Tutore immobilizzante spalla con abduzione 45°-70°

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 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number805559611ANCAEB Basic UDI-DI 08055596112226UDI-DIDate8 Jun 2026RegisteredStatusActive

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  • Withdrawn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

Trade Name
K650 Supporto anca
SK445 Tutore immobilizzante spalla con abduzione 45°-70°
Device Name
Anca
Spalla
Model / Reference
K650 Supporto anca sinistra TG XL, SK445 Tutore immobilizzante spalla con abduzione 45°-70°
Primary DI / UDI-DI
08055596112226
Basic UDI-DI
805559611ANCAEB, 805559611SPALLAMX
EMDN Code
Y061215, Y060621
Device Class
Class I
EU market of registration
Italy

Manufacturer details

EUDAMED SRN
IT-MF-000054684

Other devices from Contel S.r.l.

See all devices from Contel S.r.l. →

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