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FR-MF-00000287010801LUMBO-PERITONEAL SET is an MDD-legacy medical device registered in EUDAMED. It is classified as Class III. Manufactured by SOPHYSA. Placed on the EU market in France. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
EUDAMED last updated this device on Apr 27, 2026
B-03760124130300Primary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
(01)03760124130300
3 warnings recorded — scroll inside the panel to see all entries.
Sterile
A sterile device is supplied free of viable micro-organisms — flagged so that it is handled, stored and used to preserve that sterile state.
Single-use device
A single-use device is intended to be used on one patient during a single procedure and then discarded — not reprocessed or reused.
Contains latex
A "contains latex" flag warns that a device contains natural rubber latex, which can trigger allergic reactions in sensitive patients.
CMR substance
A CMR flag warns that a device contains a substance that is carcinogenic, mutagenic or toxic to reproduction above a defined threshold.
Endocrine-disrupting substance
An endocrine-disruptor flag warns that a device contains a substance with endocrine-disrupting properties above a defined threshold.
Primary placement in France; available across 15 countries total.
| Country | On market since | Until |
|---|---|---|
| FrancePrimary placement | Feb 1, 1990 | Still on market |
| Austria | Jun 1, 2017 | Still on market |
| Belgium | Oct 1, 2001 | Still on market |
| Bulgaria | Jun 1, 2010 | Still on market |
| Czechia | Mar 1, 2021 | Still on market |
| Germany | Dec 1, 2000 | Still on market |
| EL | Aug 1, 1999 | Still on market |
| Spain | Apr 1, 1990 | Still on market |
| Hungary | Feb 1, 2000 | Still on market |
| Ireland | Feb 1, 2020 | Still on market |
| Netherlands | May 1, 2009 | Still on market |
| Poland | Jul 1, 2005 | Still on market |
| Portugal | Mar 1, 2002 | Still on market |
| Sweden | May 1, 2025 | Still on market |
| Türkiye | Sep 1, 2000 | Still on market |
Primary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
03760124130300Basic UDI-DI
The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.
B-03760124130300LPS50UDI issuing entities
Issuing entities are the organisations the European Commission has designated to assign Unique Device Identifiers under the EU's UDI system.
MDR risk classes
MDR risk classes rank medical devices from lowest risk (Class I) to highest (Class III), which determines how much regulatory scrutiny they face.
European Medical Device Nomenclature — the EU product classification assigned to this device.
N020102SUBARACHNOID SPINAL CATHETERS AND KITSNo certificate specifically references this device's Basic UDI-DI.
No certificates registered for this manufacturer.
No certificate references this Basic UDI-DI, because: • It does not require a certificate, or • It only requires a certificate without a Basic UDI-DI reference (e.g. a QMS certificate), or • The required certificate(s) referencing this Basic UDI-DI have not been registered yet.B-03760124130072On the marketKIT PRESSIO® POUR MONITORING DE PRESSION ET DE TEMPÉRATURE INTRACRÂNIENNES, PARENCHYMATEUX À BOULONB-03760124131758On the marketKUBALA EXTERNAL VENTRICULAR CATHETER (LARGE LUMEN)B-03760124131871On the marketLUMBO-PERITONEAL SOPHY® SM8 KIT PREATTACHEDB-03760124131178On the marketPATIENT MONITOR CABLE GE DATEX OHMEDA 10 pins376012413PSOMCX000BSOn the marketPATIENT MONITOR CABLE GE SOLAR (MARQUETTE) 11 pins376012413PSOMCX000BSOn the market