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Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

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Ligaduras de Cambric sem ourela — 10 UDI-DI variants, MDR

MD Atlas
Abílio Freire Lda

Data from EUDAMED, last updated May 30, 2026

Ligaduras de Cambric sem ourela

5600710211DM106E6

10 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

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 5600710211DM106E6
Device name: Ligaduras de Cambric sem ourela
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Dec 9, 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

10 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01GKV9VQ693NKM6EAB3TW63BQG

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

DM1060505B05600710211496
DM1061007B05600710211540
DM1060507B05600710211502
DM1060515B05600710211526
DM1060510B05600710211519
DM1061010B05600710211557
DM1061515B05600710211588
DM1061020B05600710211571
DM1061015B05600710211564
DM1060520B05600710211533