Skip to content

Jalupro Biofiller Medium

by Professional Derma SA

Ref JALUPRO BIOFILLER MEDIUM

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 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-07649993836055 Basic UDI-DI 07649993836055UDI-DIDate30 Jul 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

SwedenLatviaLithuaniaGermanyPolandFranceCzech RepublicSlovakiaRomaniaSloveniaBulgariaItalyTürkiyeGreeceCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDD Active

  • Bulgaria
  • Cyprus
  • Czechia
  • France
  • Germany
  • Greece
  • Italy
  • Latvia
  • Lithuania
  • Poland
  • Romania
  • Slovakia
  • Slovenia
  • Sweden
  • Türkiye

Specification

EUDAMED

Model / Reference
JALUPRO BIOFILLER MEDIUM
Primary DI / UDI-DI
07649993836055
Basic UDI-DI
B-07649993836055
EMDN Code
P900402 Resorbable filling and reconstruction devices
Device Class
Class III
EU market of registration
Italy

Manufacturer details

EUDAMED SRN
CH-MF-000052108
Authorised representative
Quaser S.r.l. IT-AR-000008217

Other devices from Professional Derma SA

See all devices from Professional Derma SA →

Properties

  • Sterile

Other properties (10)

  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No