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Gel Knee Sleeve-Anthracite no:1

by Morsa Medi̇kal Ortopedi̇ Ve Maki̇na San. Ve Ti̇c. Ltd. Şti̇. EUDAMED

Active European Union

Ref REF-1661

Regulatory status

as of 28 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number86988110PRT160008W Basic UDI-DIDate20 Jul 2026RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not known
  • Not covered

European Union — CE/MDR Active

Certificates

0 certificates · EUDAMED

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

Specification

EUDAMED

Trade Name
Gel Knee Sleeve-Anthracite no:1
Gel Knee Sleeve-Anthracite no:3
Gel Knee Sleeve-Anthracite no:2
Device Name
Liner
Model / Reference
REF-1661
Primary DI / UDI-DI
08698811027396, 08698811027419, 08698811027402
Basic UDI-DI
86988110PRT160008W
Direct Marketing DI
08698811027396
08698811027419
08698811027402
EMDN Code
Y062499 Lower extremity prostheses - other
Device Class
Class I
Market of Registration
Türkiye

Manufacturer details

EUDAMED SRN
TR-MF-000021181

Other devices from Morsa Medi̇kal Ortopedi̇ Ve Maki̇na San. Ve Ti̇c. Ltd. Şti̇.

See all devices from Morsa Medi̇kal Ortopedi̇ Ve Maki̇na San. Ve Ti̇c. Ltd. Şti̇. →

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