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.

Assura/Alterna (Original) ostomy… — 309 UDI-DI variants, MDR

MD Atlas
Coloplast A/S

Data from EUDAMED, last updated May 23, 2026

Assura/Alterna (Original) ostomy baseplate convex

57089322976108M

309 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: Coloplast A/S

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: 57089322976108M
Device name: Assura/Alterna (Original) ostomy baseplate convex
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Feb 12, 2026

Manufacturer & authorised representative

Manufacturer

Name: Coloplast A/S
SRN: DK-MF-000025526
Country: Denmark
Email: Eudamed_PA_Contact@coloplast.com
Phone: +4549111111

Variants by status

UDI-DI variants

309 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

basicUdiUlid01KH8SK1C1MA43GVDRYJF6SQ5V

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

46746005701780455787
4675705701780414500
4676505701780414524
1428105708932535748
1427405701780935234
1426105701780900454
46757005701780455862
1272405708932164986
1271805708932164900
14263105701780958318
4674605701780414425
4676905708932191791
1272305708932164962
4674505701780477697
4676605701780477833
1428305708932344968
4675605701780414487
4676605701780414548
1426305708932156424
1426305701780935159
1426205708932156400
1427505701780935258
1426105701780999458
4676905708932154895
1427805701780935319

1 2 3 4 5