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Bonapac

by Bonanga Technology Tianjin Co., Ltd EUDAMED

Active European Union

Ref BP05Model BP02, BP03, BP04, BP05

Regulatory status

as of 26 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number697305240BA02AP Basic UDI-DIDate16 Aug 2024RegisteredStatusActive

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Certificates: none listed in EUDAMED

Specification

EUDAMED

Device Name
Bonapac
Model / Reference
BP02, BP03, BP04, BP05
Primary DI / UDI-DI
06973052403157
Basic UDI-DI
697305240BA02AP
EMDN Code
Q010304 Periodontal dressings
Device Class
Class I
Market of Registration
France

Manufacturer details

EUDAMED SRN
CN-MF-000037843
Authorised representative
SUNGO Europe B.V. NL-AR-000000247

Other devices from Bonanga Technology Tianjin Co., Ltd

See all devices from Bonanga Technology Tianjin Co., Ltd →

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