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Hegar Dilator Set

by Mehrish Industries Pvt Ltd 2 variants

Ref M15-255-257-0-14, M15-255-257-2-8

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 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/MDR Number++G410M15255257014QK Basic UDI-DI Date20 Feb 2023RegisteredStatusActive

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  • Withdrawn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/MDR Active

Specification

EUDAMED

Model / Reference
M15-255-257-0-14, M15-255-257-2-8
Primary DI / UDI-DI
G410M152552570141, G410M15255257281
Basic UDI-DI
++G410M15255257014QK, ++G410M1525525728KY
EMDN Code
L0509020101 Vaginal dilators, reusable
Device Class
Class I
EU market of registration
Romania

Manufacturer details

EUDAMED SRN
PK-MF-000031501
Authorised representative
ANTEX MEDI SOLUTION DE-AR-000008078

Other devices from Mehrish Industries Pvt Ltd

See all devices from Mehrish Industries Pvt Ltd →

Properties

  • Reusable

Other properties (12)

  • Sterile: No
  • Implantable: 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