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Careset

by Medline International France 946 variants

Ref KER72900

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 Number3666520DCSPTMISCSTWT Basic UDI-DI 03666520347130UDI-DIDate27 Apr 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  • Withdrawn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 Misc. Medical procedure pack
Model / reference
KER72900
Primary DI / UDI-DI
03666520347130
Basic UDI-DI
3666520DCSPTMISCSTWT
EMDN code
T0202 Surgical procedural kits (excluding surgical instrument kits)
Device class
Class IIa
System or procedure pack
Procedure pack
EU registration type
System or procedure pack
Medical purpose
for Misc. Medical procedure

Manufacturer details

EUDAMED SRN
FR-PR-000003713

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See all devices from Medline International France →

Properties

  • Supplied sterile

Other properties (1)

  • Sterilise before use: No