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Set de Suture

by Paul Hartmann AG 14 variants

Ref 4802291Model 3310

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 Number40495003310K7 Basic UDI-DI 04099467189195UDI-DIDate26 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  • Withdrawn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
Care set Suture / thread removal
Model / Reference
3310, 4802291
Primary DI / UDI-DI
04099467189195
Basic UDI-DI
40495003310K7
EMDN Code
H9099 Suture devices - other
Device Class
Class III
Medical Purpose
A MediSet is the compilation of defined components used to perform a medical care. The components are single-used products and are used together to perform a medical care.

Manufacturer details

EUDAMED SRN
DE-PR-000019925

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Properties

  • Sterile