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Poppi Dijon

by Prova Nova GmbH Germany EUDAMED

Ref 4152/4153/4155/4156/4712/4713/4714/4715Model Hocker EMDN Z12040280

Regulatory status

as of 26 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number4250551600000034K Basic UDI-DIDate2 Nov 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  • Withdrawn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 · synced 25 Oct 2026

Device Name
Puffi/Puffi LeMans
Model / Reference
Hocker, 4152/4153/4155/4156/4712/4713/4714/4715
Primary DI / UDI-DI
04250551699031
Basic UDI-DI
4250551600000034K
Direct Marketing DI
04250551623951
EMDN Code
Z12040280 General medicine therapeutic treatment instruments - hardware accessories
Device Class
Class I
Market of Registration
Germany

Manufacturer details

EUDAMED SRN
DE-MF-000017745

Other devices from Prova Nova GmbH

See all devices from Prova Nova GmbH →

Properties & raw data

Show properties, registry sources and raw records
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

Sources (1)

  • EUDAMED 9985ac61-6a38-41b7-a82d-8142228f879b 61 fields · synced 25 Oct 2026