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Duolith® SD1 T-Top

by Storz Medical AG Switzerland EUDAMED

Ref 21362.1001 EMDN Z12040203,Z120622,Z12101106,Z12139001,Z12169002,Z12169004

Regulatory status

as of 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number76300391ESWT006-TG Basic UDI-DIDate8 Apr 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  • Withdrawn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 · synced 24 Oct 2026

Device Name
Duolith SD1 T-Top
Model / Reference
21362.1001
Primary DI / UDI-DI
07630039101916
Basic UDI-DI
76300391ESWT006-TG
Direct Marketing DI
07630039101916
EMDN Code
Z12040203,Z120622,Z12101106,Z12139001,Z12169002,Z12169004
Device Class
Class IIb
Market of Registration
Germany

Manufacturer details

EUDAMED SRN
CH-MF-000014374
Authorised representative
STORZ MEDICAL Deutschland GmbH DE-AR-000009017

Other devices from Storz Medical AG

See all devices from Storz Medical AG →

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 07630039101916|76300391ESWT006-TG 61 fields · synced 24 Oct 2026