Skip to content

Mednetic

by Technocast Otomoti̇v Sanayi̇ Ve Ti̇c. A.Ş. Medi̇kal Şubesi̇ 165 variants

Ref PK.7.3L.20.21.35S.WT

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 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-08681645050944 Basic UDI-DI 08681645050944UDI-DIDate6 Apr 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

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDD Active

Specification

EUDAMED

Device Name
Sphincterotome 7F 3L 20mm 215cm 35GS WT
Model / Reference
PK.7.3L.20.21.35S.WT
Primary DI / UDI-DI
08681645050944
Basic UDI-DI
B-08681645050944
EMDN Code
G03040202 Papillotomes / sphincterotomes, triple (or more) lumen
Device Class
Class IIb
EU market of registration
Türkiye

Manufacturer details

EUDAMED SRN
TR-MF-000030603

Other devices from Technocast Otomoti̇v Sanayi̇ Ve Ti̇c. A.Ş. Medi̇kal Şubesi̇

See all devices from Technocast Otomoti̇v Sanayi̇ Ve Ti̇c. A.Ş. Medi̇kal Şubesi̇ →

Properties

  • Sterile

Other properties (12)

  • 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