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Bayonet Forceps (Ang. Down) 6 ½” (16.5 cm)

by Tecno Instruments (Pvt) Ltd. 2 variants

Ref 310-165-00

Active European Union

CE MDD

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 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-08964000208274 Basic UDI-DI 08964000208274UDI-DIDate12 Jun 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  • Withdrawn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/MDD Active

Specification

EUDAMED

Model / Reference
310-165-00
Primary DI / UDI-DI
08964000208274
Basic UDI-DI
B-08964000208274
EMDN Code
L180401 Open electrosurgery forceps, reusable
Device Class
Class IIb
EU market of registration
Italy

Manufacturer details

EUDAMED SRN
PK-MF-000046748
Authorised representative
Obelis s.a. BE-AR-000000106

Other devices from Tecno Instruments (Pvt.) Ltd.

See all devices from Tecno Instruments (Pvt.) Ltd. →

Properties

  • Reusable

Other properties (10)

  • Sterile: No
  • Implantable: 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