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Zuit®

by Zuitlab, Lda. EUDAMED

Withdrawn No longer placed on the EU market

Ref ZUITHDK60

Regulatory status

as of 27 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number5600208360DERMRP Basic UDI-DIDate17 Dec 2024RegisteredStatusWithdrawn No longer placed on the EU market

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Withdrawn

Certificates

0 certificates · EUDAMED

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

Specification

EUDAMED

Device Name
ZUIT® HipoDerm
Model / Reference
ZUITHDK60
Primary DI / UDI-DI
05600208360026
Basic UDI-DI
5600208360DERMRP
EMDN Code
V9099 Various devices not included in other classes - other
Device Class
Class I
Market of Registration
Portugal

Manufacturer details

EUDAMED SRN
PT-MF-000045541

Other devices from Zuitlab, Lda.

See all devices from Zuitlab, Lda. →

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