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Plasti̇-Med

by Plasti-med Plastik Medikal Ürünler San. ve Tic. Ltd. Şti. 310 variants

Ref 103 724

Plasti̇-Med (103 724) is a Class IIa device made by Plasti-med Plastik Medikal Ürünler San. ve Tic. Ltd. Şti., registered in EUDAMED on 22 Feb 2026 (Basic UDI-DI B-08698573037381), active as of 25 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 linked in EUDAMED

A group certificate may exist

Trust

Unverified

Source EUDAMED, synced 25 Oct 2026.

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-08698573037381 Basic UDI-DI 08698573037381UDI-DIDate22 Feb 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDD Active

Specification

EUDAMED

Device name
Round Silicone Drain 24 Ch
Model / reference
103 724
Primary DI / UDI-DI
08698573037381
Basic UDI-DI
B-08698573037381
EMDN code
A0601010402 Cylindrical or circular drainages (straight and t-shaped)
Device class
Class IIa
EU registration type
Legacy device (under a directive)
EU market of registration
Türkiye

Manufacturer details

EUDAMED SRN
TR-MF-000032251

Related devices

Category: Biliary drain

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Properties

  • Supplied sterile
Other properties (11, all answered No)