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Laparoscopic Nephrectomy Pack

by Johnson & Johnson Medical GmbH 3 variants

Ref LNPH39, LNPH36

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 Number0705031a030804W Basic UDI-DI Date9 Mar 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  • Withdrawn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

Model / Reference
LNPH39, LNPH36
Primary DI / UDI-DI
10705036047254, 10705036044710
Basic UDI-DI
0705031a030804W, 0705031a028355S
EMDN Code
V0599 Clinical procedures kits not included in other classes - other
Device Class
Class III
Medical Purpose
LAPAROSCOPIC NEPHRECTOMY

Manufacturer details

EUDAMED SRN
DE-PR-000035753

Related devices

Category: Ophthalmic surgical procedure kit, non-medicated, single-use

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Properties

Other properties (1)

  • Sterile: No