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Pennington Forceps

by Acheron Instruments (Private) Limited 2 variants

Ref AI-GS-02-503

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 linked in EUDAMED

A group certificate may exist

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number++G733PENNINGTON01NN Basic UDI-DI +G733AIGS025030NUDI-DIDate11 Oct 2026RegisteredStatusActive

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
Pennington Forceps
Model / Reference
AI-GS-02-503
Primary DI / UDI-DI
+G733AIGS025030N
Basic UDI-DI
++G733PENNINGTON01NN
EMDN Code
L0408020399 Intestinal forceps, reusable - other
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

Other devices from Acheron Instruments (Private) Limited

See all devices from Acheron Instruments (Private) Limited →

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