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Careset

by Medline International France 940 variants

Ref KER70018

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 Number3666520DCSPTSUTURESTH2 Basic UDI-DI 00382609822581UDI-DIDate15 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  • Withdrawn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
Sterile Suture Procedure packs
Model / Reference
KER70018
Primary DI / UDI-DI
00382609822581
Basic UDI-DI
3666520DCSPTSUTURESTH2
EMDN Code
T0202 Surgical procedural kits (excluding surgical instrument kits)
Device Class
Class IIa
Medical Purpose
For Suture Procedure

Manufacturer details

EUDAMED SRN
FR-PR-000003713

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Properties

  • Sterile