Skip to content

PerioCream Periodontal Paste

by bonyf AG EUDAMED

Active European Union

Ref 32.250.00.N.0.0.01

Regulatory status

as of 26 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number50537-60-00-03 Date30 Jul 2026IssuedStatusActive expires 18 Apr 2027

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not known
  • Not covered

European Union — CE/MDR Active

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)
  • 50537-60-00-03 Supplemented

    Quality management system EU MDR

    Notified body
    Notified body 0124
    Issued
    30 Jul 2026
    Expires
    18 Apr 2027
    Reason
    Other

Specification

EUDAMED

Model / Reference
32.250.00.N.0.0.01
Primary DI / UDI-DI
07611645329505
Basic UDI-DI
7611645PC1800JG
EMDN Code
Q010304 Periodontal dressings
Device Class
Class IIa
Market of Registration
Italy

Manufacturer details

EUDAMED SRN
LI-MF-000000739

Other devices from bonyf AG

See all devices from bonyf AG →

Properties

Show properties
Other properties (13)
  • Sterile: No
  • Implantable: No
  • 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
  • Incorporates Medicinal Product: No