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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

CLIPPER II — Class I MDR by HERDEGEN SAS

MD Atlas
HERDEGEN SAS

EUDAMED last updated this device on Apr 7, 2026

CLIPPER II

37011277Clipper1-2-3A3

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: HERDEGEN SAS
UDI-DI code: 03701127708998
Reference / catalog number: 500410

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Manufacturer information

Organization name: HERDEGEN SAS
SRN: FR-MF-000002425
Manufacturer status: Active

Critical warnings

1 warning recorded — scroll inside the panel to see all entries.

CW275
Troubles cognitifs, troubles importants de l’équilibre ou l’impossibilité de s’asseoir ou de rester assis. • Poids du patient supérieur à celui que supporte le produit. • Autres contre-indications à définir par le médecin prescripteur en fonction de l’état du patient

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: CLIPPER II
UDI-DI code: 03701127708998
Basic UDI-DI: 37011277Clipper1-2-3A3
Reference / catalog number: 500410
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: Ce rehausse WC a pour objectif principal de faciliter, sécuriser l’installation et les transferts (passage debout-assis, et inversement) sur les WC. Cette aide technique est généralement recommandée pour les personnes ayant des difficultés à se relever de leurs WC, présentant des difficultés de mobilité, un manque de force des membres inférieurs ou des troubles de la marche.
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

Y091215TOILET SEATS, RAISED

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.