Pricing Sign in

Made In Tracker

Made In Tracker EasyUDI

Legal

Privacy Policy Legal Notice

About

About FAQ Partners Contact

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

Subscribe to our monthly newsletter:

By subscribing, you accept the General Personal Data Protection Policy.

LENOSOFT — 10 UDI-DI variants, MDR (FARMABAN s.a.)

MD Atlas
FARMABAN s.a.

Data from EUDAMED, last updated May 23, 2026

LENOSOFT

8428012GUATAWL

10 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.

Sign in to open the EUDAMED record

The link to the official EUDAMED page is reserved for signed-in users. Create a free account to continue.

Email

Password

No account yet?

Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 8428012GUATAWL
Device name: LENOSOFT
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Nov 16, 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

10 UDI-DI variants

Sign in to export

Exports are reserved for signed-in users. Sign in or create an account to continue.

Email

Password

No account yet?

Export results

Applied filters

basicUdiUlid01GHGTTWGWRSH23C6SWW0WTW34

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

13229 08428012032291
1322508428012032253
1322608428012032260
13227 08428012032277
1322808428012032284
13231 08428012032314
1323308428012032338
1323408428012032345
1323208428012032321
13230 08428012032307