Skip to content

Fleximag Max 700

by Magnamed Tecnologia Medica S/A

Ref 1106630

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 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-1106630V3 Basic UDI-DI D-1106630V3UDI-DIDate13 Jul 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  • Withdrawn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

Device Name
Fleximag Max 700 - Lung Ventilator Neonate to Adult
Model / Reference
1106630
Primary DI / UDI-DI
D-1106630V3
Basic UDI-DI
B-1106630V3
EMDN Code
R9099 Respiratory and anaesthesia devices - other
Device Class
Class IIb
EU market of registration
Portugal

Manufacturer details

EUDAMED SRN
BR-MF-000013627
Authorised representative
CMC Medical Devices & Drugs SL ES-AR-000000293

Other devices from Magnamed Tecnologia Medica S/A

Properties

  • Administering Medicine

Other properties (10)

  • Sterile: No
  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No