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Brushes

by Batrik Medical Manufacturing Inc. 134 variants

Ref 311-23050F

Active European Union

CE MDR

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 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number6905210BRUSH10007A Basic UDI-DI 00690521021549UDI-DIDate19 Aug 2024RegisteredStatusActive

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  • Withdrawn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/MDR Active

Specification

EUDAMED

Device Name
Brushes
Model / Reference
311-23050F
Primary DI / UDI-DI
00690521021549
Basic UDI-DI
6905210BRUSH10007A
EMDN Code
V070101 Endoscopes cleaning brushes - for generic use
Device Class
Class I
EU market of registration
Austria

Manufacturer details

EUDAMED SRN
CA-MF-000007738
Authorised representative
Advena Limited MT-AR-000000234

Other devices from Batrik Medical Manufacturing Inc.

See all devices from Batrik Medical Manufacturing Inc. →

Properties

Other properties (13)

  • Sterile: No
  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No