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.

SenSura Flex ostomy baseplate — 117 UDI-DI variants, MDR

MD Atlas
Coloplast A/S

Data from EUDAMED, last updated May 23, 2026

SenSura Flex ostomy baseplate

57089322976078Y

117 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: 57089322976078Y
Device name: SenSura Flex ostomy baseplate
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Apr 15, 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

117 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

basicUdiUlid01KP8PFHS4F2EPS045H5KN78ZB

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

10112005708932347471
1010105708932360777
10118005708932347617
10117005708932347594
1011405708932355971
10102005708932350563
1011405708932351751
10101005708932347419
10115005708932351270
1011205708932349321
1010805708932387460
1011305708932352178
1010105708932356152
1010105708932749862
1011505708932349413
10103005708932350587
1010205708932351911
1011505708932351775
1011605708932412346
1011605708932349437
1010305701780281393
10103005708932345439
1010105708932387408
1011805708932362009
10108005708932384681

1 2 3 4 5