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Non-Sterile Single Use Bowmann Lacrimal Sinus Probe Diam 0.5/0.4mm Fig. 0000/000

by Beauty Teck International (Pvt) Ltd

Ref BTOB5000, BTOB5100

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, self-declared

Class I: no certifier involved

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-+G075BTOB50000K Basic UDI-DI Date28 Apr 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  • Withdrawn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/MDD Active

Specification

EUDAMED

Trade Name
Non-Sterile Single Use Bowmann Lacrimal Sinus Probe Diam 0.5/0.4mm Fig. 0000/000
Non-Sterile Single Use Bowmann Lacrimal Sinus Probe Diam 0.7/0.8mm Fig. 00/0
Model / Reference
BTOB5000, BTOB5100
Primary DI / UDI-DI
+G075BTOB50000K, +G075BTOB51000L
Basic UDI-DI
B-+G075BTOB50000K, B-+G075BTOB51000L
EMDN Code
K01020110 Minimally invasive surgery cannulas, single-use
Device Class
Class I
EU market of registration
Austria

Manufacturer details

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

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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