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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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MATRIX E — 5 UDI-DI variants, MDR

MD Atlas
IMO - Indústrias Metalúrgicas, S.A.

Data from EUDAMED, last updated May 30, 2026

MATRIX E

5600717213MATRIXEF7

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: IMO - Indústrias Metalúrgicas, S.A.

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 5600717213MATRIXEF7
Device name: —
Device model: MATRIX E
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Sep 12, 2023

Manufacturer & authorised representative

Manufacturer

Name: IMO - Indústrias Metalúrgicas, S.A.
SRN: PT-MF-000006644
Country: Portugal
Email: sede@imo.com.pt
Phone: +351 255 340 220

Variants by status

UDI-DI variants

5 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01HA57VGTFK2XA9WTMND2X0YAE

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

944.E405600717213028
944.E605600717213042
944.E305600717213011
944.E205600717213004
944.E505600717213035