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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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LENOPLAST — 15 UDI-DI variants, MDR (FARMABAN s.a.)

MD Atlas
FARMABAN s.a.

Data from EUDAMED, last updated May 23, 2026

LENOPLAST

8428012V202-01-10W9

15 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: FARMABAN s.a.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 8428012V202-01-10W9
Device name: LENOPLAST
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Nov 8, 2022

Manufacturer & authorised representative

Manufacturer

Name: FARMABAN s.a.
SRN: ES-MF-000004713
Country: Spain
Email: farmaban@farmaban.com
Phone: 938789507

Variants by status

UDI-DI variants

15 UDI-DI variants

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Applied filters

basicUdiUlid01GHBAZG41034AX1TRXZHYHH4G

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

8101808428012301526
8101908428012301540
81017 08428012301502
1107 08428012011074
110508428012011050
111708428012011173
1118 08428012011180
1106 08428012011067
1119 08428012011197
289075AE08428012301069
289100AE08428012301076
289050AE08428012301052
289100AI08428012301045
289075AI08428012301038
289050AI08428012301021