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Kösemed

by Kösemed Ortopedi̇ San. Ve Ti̇c. İth. İhr. A.Ş. 1,000+ variants

Ref 860-07

Kösemed (860-07) is a Class I device made by Kösemed Ortopedi̇ San. Ve Ti̇c. İth. İhr. A.Ş., registered in EUDAMED on 6 Apr 2026 (Basic UDI-DI B-86820355075367A), active as of 22 Oct 2026.

Active European Union

CE MDD

Valid until

No date given

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

Source EUDAMED, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-86820355075367A Basic UDI-DI Date6 Apr 2026RegisteredStatusActive

Official records

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  • Withdrawn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/MDD Active

Specification

EUDAMED

Device name
CCL3 Dİzüstü Burnu Açık Siyah Renk Yüksek Basınç 34-46 mmHg NO.7
CCL1 Dizüstü Burnu Kapalı Siyah RenkDüşük Basınç 18-21 mmHg NO.7
Model / reference
860-07
Primary DI / UDI-DI
D-86820355075367A, D-868203550592173
Basic UDI-DI
B-86820355075367A, B-868203550592173
EMDN code
M030405 Compression stockings
Device class
Class I
EU registration type
Legacy device (under a directive)
EU market of registration
Türkiye

Manufacturer details

EUDAMED SRN
TR-MF-000021022

Related devices

Category: Compression/pressure sock/stocking, single-use

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Other devices filed under BANDAGES.

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Properties

Other properties (12, all answered No)