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Lahey Goitre Seizing Forceps 20cm

by HILBRO International (Pvt) Ltd. EUDAMED

Active European Union

Ref 38.0034.20

Regulatory status

as of 26 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number++G27838003420NE Basic UDI-DIDate16 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  • Withdrawn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
Lahey Goitre Seizing Forceps 20cm
Model / Reference
38.0034.20
Primary DI / UDI-DI
+G2783800342008
Basic UDI-DI
++G27838003420NE
Direct Marketing DI
+G2783800342008
EMDN Code
L03130401 Tissue and organ grasping forceps, reusable
Device Class
Class I
Market of Registration
Türkiye

Manufacturer details

EUDAMED SRN
PK-MF-000025041
Authorised representative
CMC Medical Devices & Drugs SL ES-AR-000000293

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Properties

Show properties
  • Reusable
Other properties (12)
  • Sterile: No
  • Implantable: 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