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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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SOPHY® MINI MONOPRESS. VALVE MP — 1 UDI-DI variant, MDD (SOPHYSA)

MD Atlas
SOPHYSA

Data from EUDAMED, last updated Jun 2, 2026

SOPHY® MINI MONOPRESS. VALVE MP

B-03760124131079

1 UDI-DI variant

MDD [Directive 93/42/EEC on medical devices]Class III

Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class III
Manufacturer: SOPHYSA

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Device characteristics

Implantable

Legacy certificates

Certificate number: 35950
Type: refdata.legacy.mdd-certificate-type.ii-4
Notified body: GMED SAS (0459)
Validity: Jul 7, 2022

Identity & classification

Basic UDI-DI: B-03760124131079
Device name: SOPHY® MINI MONOPRESS. VALVE MP
Device model: SM1-M
Issuing agency: EUDAMED
Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class III
Version date: Apr 7, 2026

Manufacturer & authorised representative

Manufacturer

Name: SOPHYSA
SRN: FR-MF-000002870
Country: France
Email: contact@sophysa.fr
Phone: +33169351055

Variants by status

UDI-DI variants

1 UDI-DI variant

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basicUdiUlid01KNM73RYYY2JE9BK3DHNQ0KAS

Format

Summary

30 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
Market country
Issuing entity
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

SOPHY® MINI MONOPRESS. VALVE MP03760124131079