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Kit de sutura

by Medirm - Fabrico e Comércio de Dispositivos Médicos 3 variants

Ref 5521125

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 linked in EUDAMED

A group certificate may exist

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number560089748552ET Basic UDI-DI 05600897481408UDI-DIDate16 Jul 2026RegisteredStatusActive

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Model / Reference
5521125
Primary DI / UDI-DI
05600897481408
Basic UDI-DI
560089748552ET
EMDN Code
H9099 Suture devices - other
Device Class
Class IIa
Medical Purpose
O kit de sutura destina-se a ser utilizado por profissionais de saúde durante procedimentos de sutura, fornecendo um conjunto estéril de instrumentos e consumiveis necessários para o procedimento.

Manufacturer details

EUDAMED SRN
PT-PR-000002819

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Properties

  • Sterile