Skip to content

Non-Sterile Single Use Kelly Forceps Curved 160mm

by Beauty Teck International (Pvt) Ltd

Ref BTBH1355A

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 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-+G075BTBH1355A0W Basic UDI-DI +G075BTBH1355A0WUDI-DIDate26 Mar 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  • Withdrawn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

Device Name
Non-Sterile Single Use Kelly Forceps CVD 160mm
Model / Reference
BTBH1355A
Primary DI / UDI-DI
+G075BTBH1355A0W
Basic UDI-DI
B-+G075BTBH1355A0W
EMDN Code
K01020104 Minimally invasive surgery forceps, single-use
Device Class
Class IIa
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
PK-MF-000009604
Authorised representative
CMC Medical Devices & Drugs SL ES-AR-000000293

Other devices from Beauty Teck International (Pvt) Ltd

See all devices from Beauty Teck International (Pvt) Ltd →

Properties

Other properties (11)

  • Sterile: No
  • Implantable: No
  • Reusable: 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