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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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Siège de douche — 5 UDI-DI variants, MDR (PELLET ASC)

MD Atlas
PELLET ASC

Data from EUDAMED, last updated May 19, 2026

Siège de douche

356339SDERG0478ED

5 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: PELLET ASC

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 356339SDERG0478ED
Device name: Siège de douche
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Aug 29, 2025

Manufacturer & authorised representative

Manufacturer

Name: PELLET ASC
SRN: FR-MF-000041099
Country: France
Email: communication@pellet-asc.fr

Variants by status

UDI-DI variants

5 UDI-DI variants

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Applied filters

basicUdiUlid01K3TJRSWJAA2BBFPW3VKT6SG6

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

ERGONOMIC03563390478301
ERGONOMIC03563390478356
ERGONOMIC03563390478202
ERGONOMIC03563390478257
ERGONOMIC03563390478363