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Seemann Technologies

by Seemann Technologies Pakistan EUDAMED

Ref ST-99-300XXX

EMDN K0201010601

Regulatory status

as of 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number896110280TF01-014X Basic UDI-DIDate19 Aug 2025RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Not covered

European Union — CE/MDR Active

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)
  • PK25/00000133 Issued

    Quality management system EU MDR

    Notified body
    Notified body 1639
    Issued
    12 Aug 2025
    Expires
    12 Aug 2030

Specification

EUDAMED · synced 24 Oct 2026

Device Name
Sterile Single Use Bipolar Forceps
Model / Reference
ST-99-300XXX
Primary DI / UDI-DI
08961102806483
Basic UDI-DI
896110280TF01-014X
Direct Marketing DI
08961102806483
EMDN Code
K0201010601 Open electrosurgery forceps, single-use
Device Class
Class IIb
Market of Registration
Austria

Manufacturer details

EUDAMED SRN
PK-MF-000022513
Authorised representative
European Healthcare & Device Solutions Ltd. IE-AR-000003999

Other devices from Seemann Technologies

Properties & raw data

Show properties, registry sources and raw records
  • 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

Sources (1)

  • EUDAMED d81bd48f-c3ee-44b8-81fd-7f51ec55862d 61 fields · synced 24 Oct 2026