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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

GR 52 FORTISSIMO (BORDEAUX/BORDEA… — Class I MDR by VILGO

MD Atlas
VILGO

EUDAMED last updated this device on Apr 29, 2026

GR 52 FORTISSIMO (BORDEAUX/BORDEAUX)

361580GR52FORTIZQ

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: VILGO
UDI-DI code: 03615800022816
Reference / catalog number: 2020024S4

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Manufacturer information

Organization name: VILGO
SRN: FR-MF-000009712
Manufacturer status: Active

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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.

Market distribution

Primary placement in France; available across 1 country total.

Country	On market since	Until
FrancePrimary placement		Still on market

Device identification

Trade name: GR 52 FORTISSIMO (BORDEAUX/BORDEAUX)
UDI-DI code: 03615800022816
Basic UDI-DI: 361580GR52FORTIZQ
Reference / catalog number: 2020024S4
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: FAUTEUIL GR REF GR 52 FORTISSIMO BORDEAUX/BORDEAUX - CHASSIS ACIER EPOXY BORDEAUX / GARNITURE LUXE BORDEAUX / RENFORCE / A ROUES / ACCOUDOIRS ESCAMOTABLES
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

Y091203CHAIRS, TOILET AND SHOWER

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

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Expiration date
Manufacturing date
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Software identification