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Steriway

by Levent Tıbbi Cihazlar Baharat ve Şifa Bitkileri İthalat ihracat Anonim Şirketleri EUDAMED

Active European Union

Ref STWTP120350

Regulatory status

as of 27 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number8680904SH3 Basic UDI-DIDate11 May 2026RegisteredStatusActive

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  • Withdrawn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
Sterilization Products
Model / Reference
STWTP120350
Primary DI / UDI-DI
08680904003066
Basic UDI-DI
8680904SH3
Direct Marketing DI
08680904003066
EMDN Code
S01010201 Flat sterilisation pouches, tyvek/plastic film
Device Class
Class I
Market of Registration
Romania

Manufacturer details

EUDAMED SRN
TR-MF-000054014

Other devices from Levent Tıbbi Cihazlar Baharat ve Şifa Bitkileri İthalat ihracat Anonim Şirketleri

See all devices from Levent Tıbbi Cihazlar Baharat ve Şifa Bitkileri İthalat ihracat Anonim Şirketleri →

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