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Laminoitu leikkaustakki XL

by Puro Tekstiilihuoltopalvelut Oy

Ref 38971143

Withdrawn Withdrawn in European Union. No longer placed on the EU market.

Was authorized under CE MDR, withdrawn

Ended

Withdrawn

Date not published (CE MDR)

FDA recalls

Not applicable

No FDA record for this device

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number643007698002AZ Basic UDI-DI 06430076980199UDI-DIDate8 Nov 2021RegisteredStatusWithdrawn No longer placed on the EU market

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Withdrawn

Specification

EUDAMED

Device Name
Vahvistettu leikkaustakki
Model / Reference
38971143
Primary DI / UDI-DI
06430076980199
Basic UDI-DI
643007698002AZ
EMDN Code
T020402 Reinforced surgical gowns
Device Class
Class I
Medical Purpose
Vahvistettu leikkaustakki

Manufacturer details

EUDAMED SRN
FI-PR-000014539

Properties

  • Sterile