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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

HM-01 — Class I MDR by HOVERMOOV

MD Atlas
HOVERMOOV

EUDAMED last updated this device on May 8, 2026

HM-01

3770009642HMDR

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: HOVERMOOV
UDI-DI code: 03770039642003
Reference / catalog number: HM-01

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Manufacturer information

Organization name: HOVERMOOV
SRN: FR-MF-000048632
Manufacturer status: Active

Critical warnings

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

CW010
EUDAMED did not publish a description for this code.

Market distribution

Primary placement in France; available across 1 country total.

Country	On market since	Until
FrancePrimary placement	Sep 1, 2026	Still on market

Device identification

Trade name: not provided
UDI-DI code: 03770039642003
Basic UDI-DI: 3770009642HMDR
Reference / catalog number: HM-01
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: Le HM-01 est un dispositif médical de classe I d’aide à la mobilité, destiné aux personnes à mobilité réduite. Il est réservé à un usage intérieur, qui a les fonctions : D’aide à la verticalisation (se redresser et se stabiliser) D’aide au déplacement assisté (se déplacer). Le dispositif associe une fonction de verticalisation grâce à des poignées d’aide au relevage, un maintien du corps avec des appuis antébrachiaux, un maintien au niveau de la région sacrée au moyen d’une sangle, ainsi qu’un système de déplacement motorisé assisté. Il est conçu pour accompagner l’utilisateur dans les déplacements de son quotidien dans un environnement intérieur avec un diamètre de retournement réduit facilitant l’usage en espace restreint.
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: 510 MU50
850–1150 MU50
610 MU50

EMDN nomenclature code(s)

Y1299PERSONAL MOBILITY DEVICES - 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

Related devices

This device is not currently linked to any other device.

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.