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Laparoscopic Sleeve Resection Pack

by Johnson & Johnson Medical GmbH 189 variants

Ref LSR583

Laparoscopic Sleeve Resection Pack (LSR583) is a Class III device made by Johnson & Johnson Medical GmbH, registered in EUDAMED on 5 Mar 2026 (Basic UDI-DI 0705031a023354Z), active as of 25 Oct 2026.

Active European Union

CE MDR

Valid until

No date given

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

Source EUDAMED, synced 25 Oct 2026.

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number0705031a023354Z Basic UDI-DI 10705036039693UDI-DIDate5 Mar 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDR Active

Specification

EUDAMED

Model / reference
LSR583
Primary DI / UDI-DI
10705036039693
Basic UDI-DI
0705031a023354Z
EMDN code
V0599 Clinical procedures kits not included in other classes - other
Device class
Class III
System or procedure pack
Procedure pack
EU registration type
System or procedure pack
Medical purpose
LAPAROSCOPIC SLEEVE RESECTION

Manufacturer details

EUDAMED SRN
DE-PR-000035753

Related devices

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

Similar devices in this category

Other devices filed under CLINICAL PROCEDURES KITS NOT INCLUDED IN OTHER CLASSES.

Other devices from Johnson & Johnson Medical GmbH

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Properties

Other properties (2, all answered No)