Skip to content

Metal Max 90 Green System Laryngoscope Blade, Mac 2R

by PROACT Medical Ltd.

Ref MMGS90MAC2R

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 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number50560945MMGS90JF Basic UDI-DI 25056094503698UDI-DIDate30 Oct 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  • Withdrawn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
PROACT Metal Max 90 Green System Laryngoscope Blades
Model / Reference
MMGS90MAC2R
Primary DI / UDI-DI
25056094503698
Basic UDI-DI
50560945MMGS90JF
Unit of Use DI
15056094503691
EMDN Code
R9002 Laryngoscope blades, single-use
Device Class
Class I
EU market of registration
Portugal

Manufacturer details

EUDAMED SRN
GB-MF-000006294
Authorised representative
Acorn Regulatory Consultancy Services Ltd IE-AR-000000592

Other devices from PROACT Medical Ltd.

See all devices from PROACT Medical Ltd. →

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