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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 ORTOPEDICAS 100% VISCOSE — 5 UDI-DI variants, MDR

MD Atlas
A.Silva Ferreira Produtos Médicos, Lda

Data from EUDAMED, last updated May 30, 2026

LIGADURAS ORTOPEDICAS 100% VISCOSE

560086193ZIORTJJ

5 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: A.Silva Ferreira Produtos Médicos, Lda

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 560086193ZIORTJJ
Device name: LIGADURAS ORTOPEDICAS 100% VISCOSE
Device model: ZIORT
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Nov 11, 2021

Manufacturer & authorised representative

Manufacturer

Name: A.Silva Ferreira Produtos Médicos, Lda
SRN: PT-MF-000002960
Country: Portugal
Email: geral@asilvaferreira.com
Phone: 229672574

Variants by status

UDI-DI variants

5 UDI-DI variants

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Applied filters

basicUdiUlid01FM80SSBT321D975WMXKKFH1P

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

ZIORT001005600861930376
ZIORT001505600861930383
ZIORT002005600861930390
ZIORT000505600861930352
ZIORT000705600861930369