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Umbilical hernia bandage, 7 stiffening ribs

by Private Enterprise Toros-Group 10 variants

Ref Type 353- black -4Model Type 353

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 Number48201140835366 Basic UDI-DI 04820114086747UDI-DIDate25 Sep 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  • Withdrawn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

Model / Reference
Type 353, Type 353- black -4
Primary DI / UDI-DI
04820114086747
Basic UDI-DI
48201140835366
Direct Marketing DI
04820114086747
EMDN Code
Y060406 Abdominal hernia supports
Device Class
Class I
EU market of registration
Poland

Manufacturer details

EUDAMED SRN
UA-MF-000051136
Authorised representative
Medtex Sp. z o.o. PL-AR-000009252

Other devices from Private Enterprise Toros-Group

See all devices from Private Enterprise Toros-Group →

Properties

  • Contains Latex
  • Reprocessed

Other properties (11)

  • Sterile: No
  • Implantable: No
  • Reusable: 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