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Juvéderm Ultra 3

by Allergan Industrie SAS

Ref 96666-UDIModel Juvéderm Ultra 3

Active European Union

CE MDD

Valid until

Not listed

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

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-03701487900575 Basic UDI-DI 03701487900575UDI-DIDate1 Oct 2026RegisteredStatusActive

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

1 jurisdiction

NorwayIcelandSwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaLiechtensteinAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyTürkiyeCroatiaGreeceMalta
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDD Active

EU market availability

Made available in 31 countries, as listed in EUDAMED:

Declared by the manufacturer in EUDAMED for this device version; may not cover every market.

  • Austria since 7 Sep 2007
  • Belgium since 7 Sep 2007
  • Bulgaria since 7 Sep 2007
  • Croatia since 7 Sep 2007
  • Czechia since 7 Sep 2007
  • Denmark since 7 Sep 2007
  • Estonia since 7 Sep 2007
  • Finland since 7 Sep 2007
  • France since 7 Sep 2007
  • Germany since 7 Sep 2007
  • Greece since 7 Sep 2007
  • Hungary since 7 Sep 2007
  • Iceland since 7 Sep 2007
  • Ireland since 7 Sep 2007
  • Italy since 7 Sep 2007
  • Latvia since 7 Sep 2007
  • Liechtenstein since 7 Sep 2007
  • Lithuania since 7 Sep 2007
  • Luxembourg since 7 Sep 2007
  • Malta since 7 Sep 2007
  • Netherlands since 7 Sep 2007
  • Northern Ireland since 7 Sep 2007
  • Norway since 7 Sep 2007
  • Poland since 7 Sep 2007
  • Portugal since 7 Sep 2007
  • Romania since 7 Sep 2007
  • Slovakia since 7 Sep 2007
  • Slovenia since 7 Sep 2007
  • Spain since 7 Sep 2007
  • Sweden since 7 Sep 2007
  • Türkiye since 7 Sep 2007

Last checked 1 Nov 2026.

Specification

EUDAMED

Model / Reference
Juvéderm Ultra 3, 96666-UDI
Primary DI / UDI-DI
03701487900575
Basic UDI-DI
B-03701487900575
EMDN Code
P900402 Resorbable filling and reconstruction devices
Device Class
Class III
EU market of registration
France

Manufacturer details

EUDAMED SRN
FR-MF-000000490

Other devices from Allergan Industrie SAS

Properties

  • Sterile
  • Implantable
  • Incorporates Medicinal Product

Other properties (10)

  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Measuring Function: No