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EUDAMED last updated this device on Sep 14, 2023
697038963FDESD1N4Electrical stimulator is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class IIa. Manufactured by Famidoc Technology Co., Ltd.. Placed on the EU market in Malta. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
06970389634025FDES102(01)06970389634025
European Medical Device Nomenclature — the EU product classification assigned to this device.
N010103BIPOLAR NERVOUS ELECTROSTIMULATORS, BATTERY-POWERED2 warnings recorded — scroll inside the panel to see all entries.
1. Keep yourself informed of all the warnings. 2. Stimulation should not be applied over throat or mouth. Severe spasm of the laryngeal and pharyngeal muscles may occur and the contractions may be strong enough to close the airway or cause difficulty in breathing. 3. This stimulator not intended for unattended, personal use by patients who have noncompliant, emotionally disturbed, dementia, or low IQ. 4. The instruction of use was listed; any improper use may be dangerous. 5. Do not place electrodes on your head or at any sites(i.e. for head area electrode not allowed to be placed at front and back , or left and right in pairs) that may cause the electrical current to flow transcerebrally (through the head). 6. If the stimulation levels are uncomfortable or become uncomfortable, reduce the stimulation Intensity to a comfortable level and contact your physician if problems persist. 7. Never use the device in rooms where aerosols (sprays) are used or pure oxygen is being administered. 8. Do not use it near any highly flammable substances, gases or explosives. 9. Inspect Applicator cables and associated connectors before each use. 10. Turn the device off before applying or removing electrodes. 11. only use the electrode wire by the manufacturer provided or specified ,Otherwise it may cause adverse effects on the impact of product performance or patients. For replacement, please contact the manufacturer or local distributor。 12.Must be regularly examined for damage to the cord,they must not be used until the damage has been repaired
CN-MF-000016603CN23/00003635Primary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
View in glossary →The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.
OTHER
Primary placement in Malta; available across 2 countries total.
| Country | On market since | Until |
|---|---|---|
| MaltaPrimary placement | Apr 3, 2023 | Nov 11, 2099 |
| XI | Apr 3, 2023 | Nov 27, 2099 |
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 →Certificate health across this manufacturer's portfolio.
CN23/00003635AmendedNotified body
A notified body is an independent organisation, designated by an EU country, that audits manufacturers and certifies higher-risk devices before they can be CE-marked.
697038963FDESD3N8On the marketElectrical stimulator697038963FDESD3N8On the marketElectrical stimulator697038963FDESD1N4On the marketElectrical stimulator697038963FDESD3N8On the marketElectrical stimulator697038963FDESD1N4On the marketElectrical stimulator697038963FDESD1N4On the market