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Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

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LIDERFIX — 35 UDI-DI variants, MDR (LIDERMED S.A.)

MD Atlas
LIDERMED S.A.

Data from EUDAMED, last updated May 23, 2026

LIDERFIX

18426716LDFIX01LM

35 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class I

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Manufacturer: LIDERMED S.A.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 18426716LDFIX01LM
Device name: LIDERFIX
Device model: VENDAJE TUBULAR DE MALLA
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Mar 3, 2026

Manufacturer & authorised representative

Manufacturer

Name: LIDERMED S.A.
SRN: ES-MF-000004664
Country: Spain
Email: mario@lidermed.com
Phone: 663133901

Variants by status

UDI-DI variants

35 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KJSCEJCZR2SEP55TQF7K2SRJ

Format

Summary

29 columns included

Trade name
Basic UDI-DI
UDI-DI code
Risk category
Applicable legislation
Status
Organization name
SRN
Reference / catalog number
Additional product description
Intended medical purpose
Placed on the market (country)
Market info update date
Sterile
Single use
Contains latex
Reprocessed single-use
Direct marking
CMR substance
Endocrine disruptor
Annex XVI applicable
Sterilization
OEM applicable
EMDN codes
Last updated
Basic UDI-DI device name
Basic UDI-DI device model
Basic UDI-DI implantable
Basic UDI-DI reagent

003151008426716315108
003150508426716315054
003040908426716304096
003050508426716305055
003150408426716315047
003041008426716304102
003080508426716308056
003080708426716308070
003080108426716308018
003080308426716308032

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