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Topivac

by Amedus Medi̇kal Uygulamalar Sağlik Sanayi̇ Ve Ti̇caret Li̇mi̇ted Şi̇rketi̇ 3 variants

Ref ATPVSDRP3Model Multidress

Topivac (ATPVSDRP3) is a Class I device made by Amedus Medi̇kal Uygulamalar Sağlik Sanayi̇ Ve Ti̇caret Li̇mi̇ted Şi̇rketi̇, registered in EUDAMED on 28 Oct 2026 (Basic UDI-DI B-08683161110171), active as of 7 Nov 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 7 Nov 2026.

Regulatory status

as of registry sync 7 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-08683161110171 Basic UDI-DI 08683161110171UDI-DIDate28 Oct 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDD Active

Specification

EUDAMED

Device name
Medical Drape
Model / reference
Multidress, ATPVSDRP3
Primary DI / UDI-DI
08683161110171
Basic UDI-DI
B-08683161110171
EMDN code
Z12019003 Wound treatment equipment
Device class
Class I
EU registration type
Legacy device (under a directive)
EU market of registration
Latvia

Manufacturer details

EUDAMED SRN
TR-MF-000016889

Similar devices in this category

Other devices filed under WOUND TREATMENT EQUIPMENT.

Other devices from Amedus Medi̇kal Uygulamalar Sağlik Sanayi̇ Ve Ti̇caret Li̇mi̇ted Şi̇rketi̇

See all devices from Amedus Medi̇kal Uygulamalar Sağlik Sanayi̇ Ve Ti̇caret Li̇mi̇ted Şi̇rketi̇ →

Properties

  • Supplied sterile
  • Sterilise before use
Other properties (10, all answered No)