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EUDAMED last updated this device on Dec 24, 2025
843656286MIMLEDQFMIMSAL 1000 WALL is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class I. Manufactured by MIMSAL TRADE, S.L.. Placed on the EU market in Spain. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
08436562861018ML1000W(01)08436562861018
European Medical Device Nomenclature — the EU product classification assigned to this device.
Z12040199GENERAL MEDICINE DIAGNOSIS AND MONITORING INSTRUMENTS - OTHER1 warning recorded — scroll inside the panel to see all entries.
Environment 1. This device is not intended for operation in potentially explosive areas! 2. Do not use in oxygen-enriched areas! 3. Do not use near flammable anesthetic gases! 4. Do not place near strong magnetic fields such as MRI systems! 5. Do not cover the top of the lamp head! Risk of overheating! 6. In operating rooms with displacement ventilation: Do not block the ventilation with the light! 7. In the operating room with displacement ventilation: Position the light at an angle to the flow! 8. Store the light in the packaging for at least 24 hours before mounting in the room to avoid droplet formation due to condensation! Support Arm System 1. Only use the supplied support arm system for lamp suspension! 2. The entire system must be completely disconnected from the mains supply before mounting! 3. Please observe the enclosed operating instructions! 4. The support arm system is intended exclusively for the suspension of the MIMLED. Do not attach or stack other units! Electronic and optical security 1. Wh
ES-MF-000039030The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.
Primary placement in Spain; available across 5 countries total.
| Country | On market since | Until |
|---|---|---|
| SpainPrimary placement | Jan 1, 2014 | Dec 23, 2025 |
| France | Jan 1, 2014 | Dec 23, 2025 |
| Ireland | Jan 1, 2014 | Dec 23, 2025 |
| Italy | Jan 1, 2014 | Dec 23, 2025 |
| Portugal | Jan 1, 2014 | Dec 23, 2025 |
Sterile
A sterile device is supplied free of viable micro-organisms — flagged so that it is handled, stored and used to preserve that sterile state.
View in glossary →Single-use device
A single-use device is intended to be used on one patient during a single procedure and then discarded — not reprocessed or reused.
View in glossary →Contains latex
A "contains latex" flag warns that a device contains natural rubber latex, which can trigger allergic reactions in sensitive patients.
View in glossary →CMR substance
A CMR flag warns that a device contains a substance that is carcinogenic, mutagenic or toxic to reproduction above a defined threshold.
View in glossary →Endocrine-disrupting substance
An endocrine-disruptor flag warns that a device contains a substance with endocrine-disrupting properties above a defined threshold.
View in glossary →Primary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
View in glossary →Basic UDI-DI
The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.
View in glossary →UDI issuing entities
Issuing entities are the organisations the European Commission has designated to assign Unique Device Identifiers under the EU's UDI system.
View in glossary →MDR risk classes
MDR risk classes rank medical devices from lowest risk (Class I) to highest (Class III), which determines how much regulatory scrutiny they face.
View in glossary →Primary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
View in glossary →No certificate specifically references this device's Basic UDI-DI.
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.