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Sterile Single Use Hartmann Ear Specula OD 5.0mm, 38mm

by Beauty Teck International (Pvt) Ltd

Ref BTOF1122S

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 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-+G075BTOF1122S0A Basic UDI-DI +G075BTOF1122S0AUDI-DIDate18 May 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  • Withdrawn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
BTOF1122S
Primary DI / UDI-DI
+G075BTOF1122S0A
Basic UDI-DI
B-+G075BTOF1122S0A
EMDN Code
Q030312 ENT surgery spatulas, 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

Other devices from Beauty Teck International (Pvt) Ltd

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Properties

  • Sterile

Other properties (10)

  • 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