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Lats (Lats-1211)

by Shonaquip (Pty) Ltd EUDAMED

Active European Union

Ref LATS (LATS-1211)

Regulatory status

as of 26 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number6009803836LATS-SQKU Basic UDI-DIDate14 Aug 2023RegisteredStatusActive

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  • Withdrawn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
Lats
Model / Reference
LATS (LATS-1211)
Primary DI / UDI-DI
06009803836452
Basic UDI-DI
6009803836LATS-SQKU
EMDN Code
Y121821 Retractors, backrests, brackets and supports
Device Class
Class I
Market of Registration
Germany

Manufacturer details

EUDAMED SRN
ZA-MF-000036950
Authorised representative
Advena Limited MT-AR-000000234

Other devices from Shonaquip (Pty) Ltd

See all devices from Shonaquip (Pty) Ltd →

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