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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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PSPIX2 — 7 UDI-DI variants, MDR (SOPRO)

MD Atlas
SOPRO

Data from EUDAMED, last updated May 19, 2026

PSPIX2

801337602782D0001CP

7 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: SOPRO

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 801337602782D0001CP
Device name: PSPIX2
Device model: S_702_0001
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jan 26, 2026

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

7 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KFXK6442FMQDPEVQWZ13HA92

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_702_000103760278260878
S_702_000303760278260892
S_702_001303760278262421
S_702_001103760278260939
S_702_000603760278260908
S_702_001003760278260922
PSPIX203760278263688