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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

09340C — Class I MDR by MIMSAL TRADE, S.L.

MD Atlas
MIMSAL TRADE, S.L.

EUDAMED last updated this device on Dec 29, 2025

09340C

843656286LUPAPA

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: MIMSAL TRADE, S.L.
UDI-DI code: 08436562860646
Reference / catalog number: 09340C

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Manufacturer information

Organization name: MIMSAL TRADE, S.L.
SRN: ES-MF-000039030
Manufacturer status: Active

Critical warnings

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

CW010
Safety - This device is not designed to be operated in potentially explosive areas! - Do not use it in oxygen-enriched areas! - Do not use it near flammable anesthetic gases! - Do not place it close to strong magnetic fields! e.g. Magnetic resonance systems. - Do not cover the top of the lamp head! Risk of overheating! - Do not have the luminaire on for more than 8 hours at a time! - Only use the built-in power source unit! - The lighting unit does not include a fail-safe power source or an emergency battery! - In the event of a power cut, the lighting unit will shut off completely! - Short flickers are possible in the event of external EMC interference! - To switch off the lamp completely, the power plug must be removed from the outlet or the live outlet must be disabled using a separate switch. Installation and use -Luminaire with simple and ergonomic operation for intuitive handling. -Requires a MIMSAL mount, which is installed before the lamp is placed in position.

Market distribution

Primary placement in Spain; available across 1 country total.

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

Device identification

Trade name: not provided
UDI-DI code: 08436562860646
Basic UDI-DI: 843656286LUPAPA
Reference / catalog number: 09340C
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: MAGNIFIER LAMP
Additional information URL: http://www.mimsal.com/
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

Z12040199GENERAL MEDICINE DIAGNOSIS AND MONITORING INSTRUMENTS - 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

AF200 d/c LED843656286NEGATKZOn the market AF300 LED843656286NEGATKZOn the market AF400 LED843656286NEGATKZOn the market 09332-3843656286LUPAPAOn the market 09332-8843656286LUPAPAOn the market

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.