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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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SafeMatrix — 6 UDI-DI variants, MDR (Medicom SAS)

MD Atlas
Medicom SAS

Data from EUDAMED, last updated May 19, 2026

SafeMatrix

37014074DPSM01AS

6 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: Medicom SAS

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 37014074DPSM01AS
Device name: SafeMatrix
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Mar 5, 2026

Manufacturer & authorised representative

Manufacturer

Name: Medicom SAS
SRN: FR-MF-000002873
Country: France
Email: ychevalier@medicom.com

Variants by status

UDI-DI variants

6 UDI-DI variants

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Applied filters

basicUdiUlid01KJYJ917FM0BE9HPW9NMB25G7

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

SafeMatrix03700381528021
SafeMatrix03701407401021
SafeMatrix03700381528038
SafeMatrix03700381528052
SafeMatrix03700381528045
SafeMatrix03701407401045