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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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Organization name
UDI-DI code
Reference / catalog number

SELLES PIED NYLON - MOBLIER SOIN — Class I MDR by AGENCINOX SAS

MD Atlas
AGENCINOX SAS

EUDAMED last updated this device on Jan 20, 2026

SELLES PIED NYLON - MOBLIER SOIN

366710600012SELLENYLONL2

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: AGENCINOX SAS
UDI-DI code: 03667106000463
Reference / catalog number: SELLES PIED NYLON - MOBLIER SOIN

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Manufacturer information

Organization name: AGENCINOX SAS
SRN: FR-MF-000027551
Manufacturer status: Active

Market distribution

Primary placement in France; available across 1 country total.

Placed on the market in France; per-country availability dates not published.

Device identification

Trade name: not provided
UDI-DI code: 03667106000463
Basic UDI-DI: 366710600012SELLENYLONL2
Reference / catalog number: SELLES PIED NYLON - MOBLIER SOIN
Issuing entity: GS1

Classification

Risk category: Class I
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: Assise simili cuir noir montée sur colonne à gaz. Ergonomique extrêmement confortable destinée aux examens et aux travaux statiques. Idéale pour les généralistes, spécialistes, dentistes, ophtalmologues, gynécologues, kinésithérapeutes, laborantins... Cette assise permet de réduire considérablement la fatigue lombaire et les efforts musculaires par une meilleure circulation sanguine. Hauteur variable à commande manuelle de 550 à 750 mm. Équipée d’une base Nylon avec 5 roulettes jumelées ou 5 patins
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

Z12019080VARIOUS INSTRUMENTS FOR GENERAL AND MULTIDISCIPLINARY SURGERY - HARDWARE ACCESSORIES

Compliance flags

Safety

Sterile

Single use

Contains latex

Reprocessed single-use

Direct marking

Substances

CMR substance

Endocrine disruptor

Regulatory

Annex XVI applicable

Sterilization

Lifecycle

New device

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

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Certificates

No certificates registered for this manufacturer.

No certificate references this Basic UDI-DI, because: • It does not require a certificate, or • It only requires a certificate without a Basic UDI-DI reference (e.g. a QMS certificate), or • The required certificate(s) referencing this Basic UDI-DI have not been registered yet.