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Sunekos 1200

by Professional Dietetics S.p.A.

Ref DI015

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-08021756001617 Basic UDI-DI 08021756001617UDI-DIDate3 Aug 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

NorwayIcelandSwedenFinlandLatviaEstoniaDenmarkLithuaniaNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicAustriaRomaniaSloveniaBulgariaPortugalSpainItalyTürkiyeCroatiaGreece
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDD Active

EU market availability

Made available in 25 countries, as listed in EUDAMED:

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

  • Austria since 31 Jul 2015
  • Belgium since 31 Jul 2015
  • Bulgaria since 31 Jul 2015
  • Croatia since 31 Jul 2015
  • Czechia since 31 Jul 2015
  • Denmark since 31 Jul 2015
  • Estonia since 31 Jul 2015
  • Finland since 31 Jul 2015
  • France since 31 Jul 2015
  • Germany since 31 Jul 2015
  • Greece since 31 Jul 2015
  • Iceland since 31 Jul 2015
  • Italy since 23 Jun 2017
  • Latvia since 31 Jul 2015
  • Lithuania since 31 Jul 2015
  • Luxembourg since 31 Jul 2015
  • Netherlands since 31 Jul 2015
  • Norway since 31 Jul 2015
  • Poland since 31 Jul 2015
  • Portugal since 31 Jul 2015
  • Romania since 31 Jul 2015
  • Slovenia since 31 Jul 2015
  • Spain since 31 Jul 2015
  • Sweden since 31 Jul 2015
  • Türkiye since 31 Jul 2015

Last checked 25 Oct 2026.

Specification

EUDAMED

Model / Reference
DI015
Primary DI / UDI-DI
08021756001617
Basic UDI-DI
B-08021756001617
EMDN Code
P900402 Resorbable filling and reconstruction devices
Device Class
Class III
EU market of registration
Poland

Manufacturer details

EUDAMED SRN
IT-MF-000036312

Other devices from Professional Dietetics S.p.A.

See all devices from Professional Dietetics S.p.A. →

Properties

  • Sterile
  • Implantable

Other properties (9)

  • 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