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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 — 8 UDI-DI variants, MDR (PELLET ASC)

MD Atlas
PELLET ASC

Data from EUDAMED, last updated May 19, 2026

Siège de douche

356339SDCLA04768P

8 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: 356339SDCLA04768P
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

8 UDI-DI variants

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Applied filters

basicUdiUlid01K3TBNXEE0JKWQY1RZ75A1TA2

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

classic03563390476291
classic03563390476437
classic03563390476338
classic03563390476314
classic03563390476321
classic03563390476345
classic03563390476307
classic03563390476420