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Dr. Max

by Laboratorios Montplet, S.L.U. 2 variants

Ref WSMPBT002Model WSLMTI001

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 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number8413224WSLMTI001QB Basic UDI-DI 08721161755050UDI-DIDate11 Jun 2024RegisteredStatusActive

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  • Withdrawn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

Device Name
Wound Spray
Model / Reference
WSLMTI001, WSMPBT002
Primary DI / UDI-DI
08721161755050
Basic UDI-DI
8413224WSLMTI001QB
Direct Marketing DI
08721161755050
EMDN Code
V9099 Various devices not included in other classes - other
Device Class
Class IIa
EU market of registration
Czechia

Manufacturer details

EUDAMED SRN
ES-MF-000001700

Related devices

Category: Device sterilization/disinfection container, reusable

Other devices from Laboratorios Montplet, S.L.U.

Properties

  • Incorporates Medicinal Product

Other properties (12)

  • 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