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.

MOBIDERM INTIMATE — 358 UDI-DI variants, MDR

MD Atlas
Thuasne Deutschland GmbH

Data from EUDAMED, last updated May 23, 2026

MOBIDERM INTIMATE

4035459DE1201B33

358 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: Thuasne Deutschland GmbH

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: 4035459DE1201B33
Device name: MOBIDERM INTIMATE
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Dec 19, 2025

Manufacturer & authorised representative

Manufacturer

Name: Thuasne Deutschland GmbH
SRN: DE-MF-000006210
Country: Germany
Email: ra@thuasne.de

Variants by status

UDI-DI variants

358 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

basicUdiUlid01KCTZYY7F3TC60HPRK1AKN66N

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

T57155209000D6004035459373944
T571301201AAA2404035459397506
T57155210000B2604035459379847
T57154211000D7004035459373449
T57155210000E7004035459374286
T5725010900CD7004035459412872
T572301070AAA0004035459331340
T57154208500D7004035459372756
T57155211000E2604035459379953
T572302115AAA6004035459417150
T57154208500A7004035459372664
T57155209500B6004035459374033
T57154211500C7004035459373531
T5723010800DE0004035459236652
T57154209000A2604035459379380
T57154211500D2604035459379632
T57155210500D2604035459379908
T572302075AAA6004035459416566
T57155211500B2604035459379960
T57155208000B6004035459373647
T57154207500B2604035459379267
T57154211500B2604035459379618
T57154209500B7004035459372992
T57155208500D2604035459379717
T572302080AAA6004035459416658

4 5 6 7 8