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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

CEINTURE LOMBAIRE ORTHOMED PLUS — Class I MDR by MEDISPORT

MD Atlas
MEDISPORT

EUDAMED last updated this device on Feb 18, 2026

CEINTURE LOMBAIRE ORTHOMED PLUS

3664617CNT01UX

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: MEDISPORT
UDI-DI code: 03664617005604
Reference / catalog number: 864.045

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Manufacturer information

Organization name: MEDISPORT
SRN: FR-MF-000000677
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.

Critical warnings

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

CW030
EUDAMED did not publish a description for this code.

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: CEINTURE LOMBAIRE ORTHOMED PLUS
UDI-DI code: 03664617005604
Basic UDI-DI: 3664617CNT01UX
Reference / catalog number: 864.045
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: Ceinture lombaire constituée de tissu élastique aéré. Présence d’une double sangle de renfort lombaire amovible et ajustable et de passants situés sur la plaque abdominale pour une mise en place aisée. Hauteur 26 cm - Taille 4/XL
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

Y060699ORTHOSES, UPPER EXTREMITY - 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

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Expiration date
Manufacturing date
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Software identification