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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

GRENOUILLERE POUR INCONTINENCE… — Class I MDD by EMO SAS

MD Atlas
EMO SAS

EUDAMED last updated this device on Apr 17, 2025

GRENOUILLERE POUR INCONTINENCE DITE LOURDE

B-GRENOUILLEREQF

On the marketClass I

Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Organization name: EMO SAS
UDI-DI code: D-GRENOUILLEREQF
Reference / catalog number: GRENOUILLERE POUR INCONTINENCE DITE LOURDE

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Manufacturer information

Organization name: EMO SAS
SRN: FR-MF-000042150
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: GRENOUILLERE POUR INCONTINENCE DITE LOURDE
UDI-DI code: D-GRENOUILLEREQF
Basic UDI-DI: B-GRENOUILLEREQF
Reference / catalog number: GRENOUILLERE POUR INCONTINENCE DITE LOURDE
Issuing entity: EUDAMED

Classification

Risk category: Class I
Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: Grenouillère médicalisée pour faciliter l'habillement des personnes dépendantes. La fermeture se fermant dans le haut du dos, il est impossible pour les personnes dépendantes d'y accéder et de se déshabiller. Les tissus 100% coton sont labellisés "FRANCE TERRE TEXTILE". Les tissus sont teints avec des colorants strictement conformes aux normes européennes et certifiés Oeko Tex Standard 100.
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

V9099VARIOUS DEVICES NOT INCLUDED IN OTHER CLASSES - OTHER

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.