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General Surgery Procedure Pack

by Covidien llc 564 variants

Ref KITLAPSJC0001

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 Number0763000B00008848N Basic UDI-DI 00824846025795UDI-DIDate28 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  • Withdrawn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
General Surgery Procedure Pack
Model / Reference
KITLAPSJC0001
Primary DI / UDI-DI
00824846025795
Basic UDI-DI
0763000B00008848N
EMDN Code
V9099 Various devices not included in other classes - other
Device Class
Class III
Medical Purpose
Обща хирургия

Manufacturer details

EUDAMED SRN
US-PR-000013794

Other devices from Covidien llc

See all devices from Covidien llc →

Properties

Other properties (1)

  • Sterile: No