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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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LENOTAPE — 4 UDI-DI variants, MDR (FARMABAN s.a.)

MD Atlas
FARMABAN s.a.

Data from EUDAMED, last updated May 23, 2026

LENOTAPE

8428012ESPARADRAPYW

4 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: 8428012ESPARADRAPYW
Device name: LENOTAPE
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Nov 11, 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

4 UDI-DI variants

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Applied filters

basicUdiUlid01GHGYG3P7V08SJGVPPEZJ51EH

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

401108428012303230
135108428012013511
135008428012013504
135208428012013528