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Careset

by Medline International France 547 variants

Ref KER70009A

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 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number3666520DCSPTSKIPRESTIEC Basic UDI-DI 00382609892485UDI-DIDate29 May 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  • Withdrawn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
Sterile Skin preparation set
Model / Reference
KER70009A
Primary DI / UDI-DI
00382609892485
Basic UDI-DI
3666520DCSPTSKIPRESTIEC
EMDN Code
T0202 Surgical procedural kits (excluding surgical instrument kits)
Device Class
Class I
Medical Purpose
For Skin preparation

Manufacturer details

EUDAMED SRN
FR-PR-000003713

Other devices from Medline International France

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Properties

  • Sterile