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PharmaCare Hernia Belt

by Irufa Industrial Group CO., LTD. EUDAMED

Active European Union

Ref Hernia Belt MModel Hernia Belt

Regulatory status

as of 28 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number0471996166Hernia4Z Basic UDI-DIDate15 Aug 2026RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not known
  • Not covered

European Union — CE/MDR Active

Certificates

0 certificates · EUDAMED

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

Specification

EUDAMED

Device Name
Hernia Belt
Model / Reference
Hernia Belt, Hernia Belt M
Primary DI / UDI-DI
00767062223036
Basic UDI-DI
0471996166Hernia4Z
EMDN Code
Y060406 Abdominal hernia supports
Device Class
Class I
Market of Registration
Ireland

Manufacturer details

EUDAMED SRN
TW-MF-000046083
Authorised representative
KHANG BAO INTERNATIONAL KFT HU-AR-000034102

From the manufacturer

Manufacturer's product page: Hernia Belts

Other devices from Irufa Industrial Group CO., LTD.

See all devices from Irufa Industrial Group CO., LTD. →

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