Skip to content

Fides

by Fabryka Materacy Janpol Sp. z o.o. EUDAMED

Active European Union

Ref MAT-FRE-XXXXXXXX-XXXXModel materac rehabilitacyjnych

Regulatory status

as of 29 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-MAT-FRE-XXXXXXXX-XXXXNZ Basic UDI-DIDate14 Sep 2026RegisteredStatusActive

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDD Active

Certificates

0 certificates · EUDAMED

No notified-body certificate is listed. Devices of this class are self-declared by the manufacturer.

Specification

EUDAMED

Model / Reference
materac rehabilitacyjnych, MAT-FRE-XXXXXXXX-XXXX
Primary DI / UDI-DI
D-MAT-FRE-XXXXXXXX-XXXXNZ
Basic UDI-DI
B-MAT-FRE-XXXXXXXX-XXXXNZ
EMDN Code
V0899 Medical support equipment - other
Device Class
Class I
Market of Registration
Poland

Manufacturer details

EUDAMED SRN
PL-MF-000051814

Other devices from Fabryka Materacy Janpol Sp. z o.o.

See all devices from Fabryka Materacy Janpol Sp. z o.o. →

Properties

  • Contains Latex

Other properties (10)

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