Skip to content

Non-Sterile Single Use Allis Tissue Grasping Forceps 200mm 6x7 teeth

by Beauty Teck International (Pvt) Ltd

Ref BTEA0200

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-+G075BTEA020006 Basic UDI-DI +G075BTEA020006UDI-DIDate16 Apr 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  • Withdrawn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
BTEA0200
Primary DI / UDI-DI
+G075BTEA020006
Basic UDI-DI
B-+G075BTEA020006
EMDN Code
K01020104 Minimally invasive surgery forceps, single-use
Device Class
Class IIa
EU market of registration
Austria

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