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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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SOPIX2 — 15 UDI-DI variants, MDR (SOPRO)

MD Atlas
SOPRO

Data from EUDAMED, last updated May 19, 2026

SOPIX2

801337602782D0009D7

15 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class IIa

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: SOPRO

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 801337602782D0009D7
Device name: SOPIX2
Device model: S_802_0001.
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Jul 9, 2024

Manufacturer & authorised representative

Manufacturer

Name: SOPRO
SRN: FR-MF-000000833
Country: France
Email: info@sopro.acteongroup.com
Phone: +33 4 42 98 01 01

Variants by status

UDI-DI variants

15 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01J2BNX1AHZ03MA7KQCR2HT56K

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

S_802_0011.03760278264111
SOPIX203760278262681
S_802_000303760278264050
S_802_001603760278263459
S_802_001503760278266092
S_802_000403760278264067
S_802_001303760278263381
S_802_001203760278263374
S_802_001703760278263466
S_802_000803760278262674
S_802_001403760278263794
S_802_000703760278264098
S_802_000503760278264074
S_802_0001.03760278264043
S_802_000603760278264081