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Schiller

by Schiller Medical 10 variants

Ref 1-58-9100

Schiller (1-58-9100) is a Class IIb device made by Schiller Medical, registered in EUDAMED on 1 Dec 2022 (Basic UDI-DI B-07613365900491), 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-07613365900491 Basic UDI-DI 07613365900491UDI-DIDate1 Dec 2022RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDD Active

Specification

EUDAMED

Device name
FRED easy automatique
Model / reference
1-58-9100
Primary DI / UDI-DI
07613365900491
Basic UDI-DI
B-07613365900491
EMDN code
Z12030503 Automatic defibrillators
Device class
Class IIb
EU registration type
Legacy device (under a directive)
EU market of registration
France

Manufacturer details

EUDAMED SRN
FR-MF-000003190

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Other devices filed under AUTOMATIC DEFIBRILLATORS.

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Properties

Other properties (12, all answered No)