Pricing Sign in

Made In Tracker

Made In Tracker EasyUDI

Legal

Privacy Policy Legal Notice

About

About FAQ Partners Contact

Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

Subscribe to our monthly newsletter:

By subscribing, you accept the General Personal Data Protection Policy.

SOFLEX — 6 UDI-DI variants, MDR (France Reval)

MD Atlas
France Reval

Data from EUDAMED, last updated May 19, 2026

SOFLEX

3666401DC006JZ

6 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: France Reval

Sign in to open the EUDAMED record

The link to the official EUDAMED page is reserved for signed-in users. Create a free account to continue.

Email

Password

No account yet?

Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 3666401DC006JZ
Device name: SOFLEX
Device model: FAUTEUIL ELEVATEUR DE DOUCHE
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jan 8, 2026

Manufacturer & authorised representative

Manufacturer

Name: France Reval
SRN: FR-MF-000011523
Country: France
Email: responsablequalite@france-reval.com
Phone: +33 5 46 42 04 16

Variants by status

UDI-DI variants

6 UDI-DI variants

Sign in to export

Exports are reserved for signed-in users. Sign in or create an account to continue.

Email

Password

No account yet?

Export results

Applied filters

basicUdiUlid01KEEVHGR0DR23M6E7NWZT7XDE

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

FLEXO HYDRAULIQUE36664010014270
FLEXO HYDRAULIQUE36664010014348
SOFLEX ELECTRIQUE36664010014652
SOFLEX ELECTRIQUE36664010014584
SOFLEX HYDRAULIQUE36664010014416
SOFLEX HYDRAULIQUE36664010001300