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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

Châssis CS210 — Class I MDR by OBRO

MD Atlas
OBRO

EUDAMED last updated this device on Jun 4, 2024

Châssis CS210

376039415050C5

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: OBRO
UDI-DI code: 03760394150541
Reference / catalog number: CS210

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Manufacturer information

Organization name: OBRO
SRN: FR-MF-000019841
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.

Placed on the market in France; per-country availability dates not published.

Device identification

Trade name: Châssis CS210
UDI-DI code: 03760394150541
Basic UDI-DI: 376039415050C5
Reference / catalog number: CS210
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: • Base de verticalisation • Excellente stabilité • Réglage facile et rapide • Vérin réglable en poussée ou en tirant • Support de pied réglable sur 3 axes • Support de mollet réglable sur 3 axes • Porte tablette et anti-bascule en option
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

Z12130202TRACTION SYSTEMS

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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Manufacturing date
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Software identification