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Juvapen Expert

by Juvaplus SA

Ref JPE01Model Juvapen Expert

Juvapen Expert (JPE01) is a Class IIa device made by Juvaplus SA, registered in EUDAMED on 11 Apr 2022 (Basic UDI-DI B-++EJUVJPE01BY), 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-++EJUVJPE01BY Basic UDI-DI ++EJUVJPE01BYUDI-DIDate11 Apr 2022RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDD Active

Specification

EUDAMED

Device name
JPE01
Model / reference
Juvapen Expert, JPE01
Primary DI / UDI-DI
++EJUVJPE01BY
Basic UDI-DI
B-++EJUVJPE01BY
EMDN code
A99 Devices for administration, withdrawal and collection - other
Device class
Class IIa
System or procedure pack
Procedure pack which is a device in itself
EU registration type
Legacy device (under a directive)
EU market of registration
France

Manufacturer details

EUDAMED SRN
CH-MF-000017503
Authorised representative
EUSwissMed GmbH DE-AR-000016945

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Properties

Other properties (12, all answered No)