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Liderfix

by Lidermed S.A. 18 variants

Part of a family of 20 devices: see the family page

Ref 0030505Model VENDAJE TUBULAR DE MALLA

Liderfix (0030505) is a Class I device made by Lidermed S.A., registered in EUDAMED on 3 Mar 2026 (Basic UDI-DI 18426716LDFIX01LM), active as of 25 Oct 2026.

Active European Union

CE MDR

Valid until

No date given

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

Source EUDAMED, synced 25 Oct 2026.

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number18426716LDFIX01LM Basic UDI-DI 08426716305055UDI-DIDate3 Mar 2026RegisteredStatusActive

Official records

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  • Withdrawn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

Model / reference
VENDAJE TUBULAR DE MALLA, 0030505
Primary DI / UDI-DI
08426716305055
Basic UDI-DI
18426716LDFIX01LM
Direct marketing DI
08426716305055
EMDN code
M03030103 Tubular net bandages
Device class
Class I
System or procedure pack
System which is a device in itself
EU registration type
Standard device
EU market of registration
Spain

Manufacturer details

EUDAMED SRN
ES-MF-000004664

Similar devices in this category

Other devices filed under TUBULAR NET BANDAGES.

Other devices from Lidermed S.A.

See all devices from Lidermed S.A. →

Properties

Other properties (14, all answered No)