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Juvapen Toxin

by Juvaplus SA

Ref JP01

Juvapen Toxin (JP01) is a Class IIa device made by Juvaplus SA, registered in EUDAMED on 4 Apr 2022 (Basic UDI-DI B-++EJUVJP01DG), 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-++EJUVJP01DG Basic UDI-DI ++EJUVJP01DGUDI-DIDate4 Apr 2022RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDD Active

Specification

EUDAMED

Model / reference
JP01
Primary DI / UDI-DI
++EJUVJP01DG
Basic UDI-DI
B-++EJUVJP01DG
EMDN code
A99 Devices for administration, withdrawal and collection - other
Device class
Class IIa
System or procedure pack
System which is a device in itself
EU registration type
Legacy device (under a directive)
EU market of registration
Norway

Manufacturer details

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

Similar devices in this category

Other devices filed under DEVICES FOR ADMINISTRATION, WITHDRAWAL AND COLLECTION - OTHER.

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Properties

  • Administering medicine
Other properties (11, all answered No)