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SF160

by Memmert GmbH + Co.KG

Ref SF160

SF160 is a Class IIb device made by Memmert GmbH + Co.KG, registered in EUDAMED on 8 Jun 2026 (Basic UDI-DI B-04251817501655), active as of 22 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-04251817501655 Basic UDI-DI 04251817501655UDI-DIDate8 Jun 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDD Active

Specification

EUDAMED

Device name
SF160
Model / reference
SF160
Primary DI / UDI-DI
04251817501655
Basic UDI-DI
B-04251817501655
EMDN code
S9099 Sterilisation devices (excluding cat. d - z) - other
Device class
Class IIb
EU registration type
Legacy device (under a directive)
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
DE-MF-000012127

Similar devices in this category

Other devices filed under STERILISATION DEVICES (EXCLUDING CAT. D - Z) - OTHER.

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Properties

Other properties (12, all answered No)