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Pergo

by Pergo Medikal ve Ilac Sanayi A.S. 119 variants

Ref 05TD3822

Active European Union

CE MDD

Valid until

Not listed

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

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-08682952402082 Basic UDI-DI 08682952402082UDI-DIDate14 May 2026RegisteredStatusActive

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  • Withdrawn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/MDD Active

Specification

EUDAMED

Device Name
Sterile Closed Suction System Double Lumen 7 Ch
Model / Reference
05TD3822
Primary DI / UDI-DI
08682952402082
Basic UDI-DI
B-08682952402082
EMDN Code
A0601010299 Drainage systems with adjustable suction - other
Device Class
Class IIa
EU market of registration
Austria

Manufacturer details

EUDAMED SRN
TR-MF-000020761

Other devices from Pergo Medikal ve Ilac Sanayi A.S.

See all devices from Pergo Medikal ve Ilac Sanayi A.S. →

Properties

  • Sterile

Other properties (10)

  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No