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Goulian Skin Graft Knife Set

by Acheron Instruments (Private) Limited

Ref AI-GS-01-013

Active European Union

CE MDR

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None, self-declared

Class I: no certifier involved

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number++G733SKINGRAFTSET01UR Basic UDI-DI +G733AIGS010130IUDI-DIDate3 Oct 2026RegisteredStatusActive

Certificates

0 certificates · EUDAMED

No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
Goulian Skin Graft Knife Set
Model / Reference
AI-GS-01-013
Primary DI / UDI-DI
+G733AIGS010130I
Basic UDI-DI
++G733SKINGRAFTSET01UR
EMDN Code
L0103 Dermotomes and blades, reusable
Device Class
Class I
EU market of registration
Hungary

Manufacturer details

EUDAMED SRN
PK-MF-000037497
Authorised representative
KHANG BAO INTERNATIONAL KFT HU-AR-000034102

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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