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.

Ligadura Elástica Tipo Crepe 4m x 5cm — 12 UDI-DI variants, MDR

MD Atlas
Abílio Freire Lda

Data from EUDAMED, last updated May 30, 2026

Ligadura Elástica Tipo Crepe 4m x 5cm

5600710211DM101DU

12 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: Abílio Freire Lda

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: 5600710211DM101DU
Device name: Ligadura Elástica Tipo Crepe 4m x 5cm
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Aug 4, 2022

Manufacturer & authorised representative

Manufacturer

Name: Abílio Freire Lda
SRN: PT-MF-000022553
Country: Portugal
Email: geral@afreire.com
Phone: +351255878497

Variants by status

UDI-DI variants

12 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

basicUdiUlid01G9MTK0BGCT4M0BHE8KJ37YMK

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

DM1010407B05600710211014
DM1010505B05600710211069
DM1010415B05600710211045
DM1010405B05600710211007
DM1011015B05600710211113
DM1010520B05600710211090
DM1010410B05600710211021
DM1011010B05600710211106
DM1010510B05600710211076
DM1010515B05600710211083
DM1010420B05600710211052
DM1011020B05600710211120