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Ankalaps-Woop

by Anka Sağlık Gereçleri San. İç ve Dış Tic. Ltd. Şti. Türkiye EUDAMED

Ref AIPXL-HS

EMDN K01020106

Regulatory status

as of 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-08680395535299 Basic UDI-DIDate18 May 2026RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Expiring (legacy directive)
  • Not covered

European Union — CE/MDD Expiring (legacy directive)

Certificates: none listed in EUDAMED

Specification

EUDAMED · synced 24 Oct 2026

Device Name
Incision Protector Retractor - XL-HS
Model / Reference
AIPXL-HS
Primary DI / UDI-DI
08680395535299
Basic UDI-DI
B-08680395535299
EMDN Code
K01020106 Minimally invasive surgery spreaders and retractors, single-use
Device Class
Class IIa
Market of Registration
Türkiye

Manufacturer details

EUDAMED SRN
TR-MF-000022980

Other devices from Anka Sağlık Gereçleri San. İç ve Dış Tic. Ltd. Şti.

See all devices from Anka Sağlık Gereçleri San. İç ve Dış Tic. Ltd. Şti. →

Properties & raw data

Show properties, registry sources and raw records
  • Sterile
Other properties (10)
  • Implantable: No
  • 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

Sources (1)

  • EUDAMED 4b2f2a03-3549-466a-bbd1-42996e24cab8 61 fields · synced 24 Oct 2026