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.

Templates — 624 UDI-DI variants, MDR (Medartis AG)

MD Atlas
Medartis AG

Data from EUDAMED, last updated May 23, 2026

Templates

76300378005PA

624 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: Medartis 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

Reusable

Identity & classification

Basic UDI-DI: 76300378005PA
Device name: Templates
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Apr 22, 2026

Manufacturer & authorised representative

Manufacturer

Name: Medartis AG
SRN: CH-MF-000022291
Country: Switzerland
Email: mario.dellacasa@medartis.com
Phone: +41 61 633 3565

Authorised representative

Name: Medartis GmbH
SRN: DE-AR-000005810
Country: Germany
Phone: +49 7665 98 24 0

Variants by status

UDI-DI variants

624 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

basicUdiUlid01KPTCGX1E3F6HGHHGWQAJDX21

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

Template for A-4650.6707630894814600
Template for A-4650.6707630037897569
Template for A-4650.6907630894813283
Template for A-4650.9107630894813344
Template for A-4655.0107630037897576
Template for A-4655.0107630894814013
Template for A-4655.0207630037897583
Template for A-4655.0207630894814617
Template for A-4655.0307630037897590
Template for A-4655.0307630894814624
Template for A-4655.0807630894814631
Template for A-4655.0807630037897606
Template for A-4655.0907630894813375
Template for A-4655.1007630894814648
Template for A-4655.1007630037897613
Template for A-4655.1107630894814655
Template for A-4655.1107630037897620
Template for A-4655.1207630037897637
Template for A-4655.1207630894814662
Template for A-4655.1307630037897644
Template for A-4655.1307630894814679
Template for A-4655.1507630894813405
Template for A-4655.1607630037897651
Template for A-4655.1607630894814686
Template for A-4655.1707630037897668

4 5 6 7 8