Skip to content

GM501 Flush

by Gynemed GmbH & Co. KG EUDAMED

Active European Union

Ref 4 GM 501F-50, 4 GM 501F-500

Regulatory status

as of 26 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-04260173190779 Basic UDI-DIDate29 Oct 2025RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not known
  • Not covered

European Union — CE/MDD Expiring

Certificates: none listed in EUDAMED

Specification

EUDAMED

Trade Name
GM501 Flush
GM501 Flush 500 ml
Model / Reference
4 GM 501F-50, 4 GM 501F-500
Primary DI / UDI-DI
04260173190779, 04260173192490
Basic UDI-DI
B-04260173190779, B-04260173192490
EMDN Code
U08020502 Materials/solutions for preparation/handling for assisted reproduction
Device Class
Class III
Market of Registration
Germany

Manufacturer details

EUDAMED SRN
DE-MF-000005264

Other devices from Gynemed GmbH & Co. KG

See all devices from Gynemed GmbH & Co. KG →

Properties

Show properties
  • Sterile
  • Animal Tissues
Other properties (9)
  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • Human-derived: No
  • Human Tissues: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No