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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

MSB010.CX3 — IVDR Class A IVDR by MEDICAL SCIENTIFIC…

MD Atlas
MEDICAL SCIENTIFIC EQUIPMENT

EUDAMED last updated this device on Aug 21, 2023

MSB010.CX3

3770031977MSB010.CX3C4

On the marketIVDR Class A

Applicable legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Organization name: MEDICAL SCIENTIFIC EQUIPMENT
UDI-DI code: 03770031977028
Reference / catalog number: MSB010.CX3

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Manufacturer information

Organization name: MEDICAL SCIENTIFIC EQUIPMENT
SRN: FR-MF-000025224
Manufacturer status: Active

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Critical warnings

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

CW010
Always consult instruction before first use

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: not provided
UDI-DI code: 03770031977028
Basic UDI-DI: 3770031977MSB010.CX3C4
Reference / catalog number: MSB010.CX3
Issuing entity: GS1

Classification

Risk category: IVDR Class A
Applicable legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: Small centrifuge, ventilated, table laboratory centrifuge, intended for basic applications and sample preparation. With minimal dimensions it provides the ease of use, allowing for quick and accurate separation of various liquid. It was designed specifically for the needs of small medical laboratories and veterinary clinics or cabinets, in which you can often centrifuge from one to several tubes at the same time. Mainly dedicated for 1.5/2ml and capillaries tubes and pcr strips.
Additional information URL: https://mse-sas.com/
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

W02069003CENTRIFUGES

Compliance flags

Safety

Sterile

Single use

Direct marking

Regulatory

Sterilization

Lifecycle

New device

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

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.