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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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Soufflet — 2 UDI-DI variants, MDR (Leved)

MD Atlas
Leved

Data from EUDAMED, last updated May 19, 2026

Soufflet

3770038614S5SOUF20252P

2 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: Leved

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 3770038614S5SOUF20252P
Device name: —
Device model: Soufflet
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Apr 11, 2025

Manufacturer & authorised representative

Manufacturer

Name: Leved
SRN: FR-MF-000047070
Country: France
Email: edouard.leveque@leved.com
Phone: 0668085900

Variants by status

UDI-DI variants

2 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01JRJ9P3PRXCA61RWWV4DECK3M

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

LEVED03770038614056
Soufflet S503770038614049