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Lap Protector - FF1010H

by Hakko Co., Ltd.

Ref FF1010H

Lap Protector - FF1010H is a Class IIa device made by Hakko Co., Ltd., registered in EUDAMED on 26 May 2026 (Basic UDI-DI B-04526737191027), active as of 24 Oct 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 24 Oct 2026.

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-04526737191027 Basic UDI-DI 04526737191027UDI-DIDate26 May 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDD Active

Specification

EUDAMED

Device name
Lap Protector - FF1010H
Model / reference
FF1010H
Primary DI / UDI-DI
04526737191027
Basic UDI-DI
B-04526737191027
EMDN code
K01020106 Minimally invasive surgery spreaders and retractors, single-use
Device class
Class IIa
EU registration type
Legacy device (under a directive)
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
JP-MF-000010711
Authorised representative
MDSS GmbH DE-AR-000005430

Similar devices in this category

Other devices filed under MINIMALLY INVASIVE SURGERY SPREADERS AND RETRACTORS, SINGLE-USE.

Other devices from Hakko Co., Ltd.

See all devices from Hakko Co., Ltd. →

Properties

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