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Kit De Specialite

by France Partenaires Medical 3 variants

Ref ACC21D

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 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number376037126/SPE-2YM Basic UDI-DI 03760371260928UDI-DIDate12 Jun 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  • Withdrawn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

Device Name
Kit De Specialite
Model / Reference
ACC21D
Primary DI / UDI-DI
03760371260928
Basic UDI-DI
376037126/SPE-2YM
EMDN Code
V9099 Various devices not included in other classes - other
Device Class
Class IIa
Medical Purpose
Kit de spécialité

Manufacturer details

EUDAMED SRN
FR-PR-000016364

Other devices from France Partenaires Medical

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Properties

  • Sterile