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Maxmore Spine

by Kirwan Surgical Products LLC

Ref 1001-MDE 003

Maxmore Spine (1001-MDE 003) is a Class IIb device made by Kirwan Surgical Products LLC, registered in EUDAMED on 27 Oct 2026 (Basic UDI-DI B-00841019122150), active as of 7 Nov 2026.

Active European Union

CE MDD

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/MDD NumberB-00841019122150 Basic UDI-DI 00841019122150UDI-DIDate27 Oct 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDD Active

Specification

EUDAMED

Device name
Disposable Dual Tip Electrode
Model / reference
1001-MDE 003
Primary DI / UDI-DI
00841019122150
Basic UDI-DI
B-00841019122150
EMDN code
K0201010501 Open electrosurgery handpieces, single-use
Device class
Class IIb
System or procedure pack
System which is a device in itself
EU registration type
Legacy device (under a directive)
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
US-MF-000008222
Authorised representative
MPS Medical Product Service GmbH DE-AR-000005009

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  • Kirwan 20-1110AUS

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  • Kirwan 10-1413AUS

    Class II

See all devices from Kirwan Surgical Products LLC →

Properties

  • Supplied sterile
Other properties (11, all answered No)