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.

Anti Dekubitus Matratze — 421 UDI-DI variants, MDR (OBA AG)

MD Atlas
OBA AG

Data from EUDAMED, last updated May 23, 2026

Anti Dekubitus Matratze

76303184ADMV9

421 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: OBA AG

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: 76303184ADMV9
Device name: Anti Dekubitus Matratze
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jan 29, 2025

Manufacturer & authorised representative

Manufacturer

Name: OBA AG
SRN: CH-MF-000037383
Country: Switzerland
Email: info@oba.ch

Authorised representative

Name: ANNIE BAUER CONFORT
SRN: FR-AR-000037165
Country: France
Phone: +33493229475

Variants by status

UDI-DI variants

421 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

basicUdiUlid01H959BQ6QNDR1F1JGBBJ76Y3J

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

3008.10607630318402727
3008.40107630318402970
3008.50807630318403144
3008.11307630318403199
3008.000.00307630318402673
3008.20307630318402796
3008.50607630318403120
3008.20707630318402833
3008.40907630318403052
3008.20107630318402772
3008.10207630318402680
3008.20907630318402857
3008.30507630318402918
3008.11107630318403175
3008.20207630318402789
3008.40607630318403021
3008.41007630318403069
3008.20807630318402840
3008.21007630318402864
3008.30907630318402956
3008.40207630318402987
3008.10707630318402734
3008.11407630318403205
3008.20607630318402826
3008.50207630318403083