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Vats Lobectomy Procedure Pack

by Johnson & Johnson Medical GmbH 103 variants

Ref VATS210

Vats Lobectomy Procedure Pack (VATS210) is a Class III device made by Johnson & Johnson Medical GmbH, registered in EUDAMED on 5 Nov 2026 (Basic UDI-DI 0705031a036185P), active as of 7 Nov 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 7 Nov 2026.

Regulatory status

as of registry sync 7 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number0705031a036185P Basic UDI-DI 10705036052838UDI-DIDate5 Nov 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Model / reference
VATS210
Primary DI / UDI-DI
10705036052838
Basic UDI-DI
0705031a036185P
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
VATS LOBECTOMY PROCEDURE

Manufacturer details

EUDAMED SRN
DE-PR-000035753

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)