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PT 0121/22 Ostomy abdominal belt with a panel for individual location of the opening 22, XXXL

by Sigvaris Spółka Akcyjna

Ref 121/22XXXLModel PT 0121/22 Stomijny pas brzuszny z panelem do indywidualnej lokalizacji otworu „22”

Active European Union

CE MDR

Valid until

Not listed

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

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number5906699PT0121/22WZ Basic UDI-DI 05906699067247UDI-DIDate9 Jul 2026RegisteredStatusActive

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  • Withdrawn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/MDR Active

Specification

EUDAMED

Device Name
PT 0121/22 Stomijny pas brzuszny z panelem do indywidualnej lokalizacji otworu „22”
Model / Reference
PT 0121/22 Stomijny pas brzuszny z panelem do indywidualnej lokalizacji otworu „22”, 121/22XXXL
Primary DI / UDI-DI
05906699067247
Basic UDI-DI
5906699PT0121/22WZ
EMDN Code
Y060403 Abdominal muscles supports
Device Class
Class I
EU market of registration
Poland

Manufacturer details

EUDAMED SRN
PL-MF-000004824

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Properties

Other properties (13)

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