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EUDAMED last updated this device on Apr 21, 2026
376007674MIGSPRAY8MMIG SPRAY is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class IIa. Manufactured by VITROBIO SAS. Placed on the EU market in France. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
03760076742576VPF MIG - 06 MDR(01)03760076742576
European Medical Device Nomenclature — the EU product classification assigned to this device.
Q030199NASOPHARYNGEAL DEVICES - OTHER10 warnings recorded — scroll inside the panel to see all entries.
Warning and precautions: In the absence of sufficient safety data, MIG SPRAY is contraindicated in the cases listed below. If you still intend to use MIG SPRAY in any of these cases, we strongly advise you to speak to your doctor or pharmacist. •If you have an history of cluster or hemiplegic headache. •If you have chronic migraine (>15 migraine days per month). •If you have major mental or psychiatric disorder. •If you have a history of seizure. •If you have active chronic pain syndrome. •If you have cardiac or hepatic disease. •If you have problems with your nose or nasal septum (e.g. septal deviation or nasal polyposis). •If there is a confirmed or suspected viral infection in children. •If you are a pregnant or breastfeeding women. •Children under the age of seven (7) years old. Children: MIG SPRAY may be used by children over the age of seven (7) under adult supervision. To monitor the progress of your child's migraines, it is strongly recommended that you have regular check-ups with your child's doctor. If you have any doubts before starting treatment or if you experience any side effects, you should consult your doctor. Important Notice: If you are experiencing a severe headache for the first time, or if you have not been diagnosed with migraines, do not use MIG SPRAY. Please consult your doctor promptly to determine the cause of your headache.
Primary placement in France; available across 1 country total.
| Country | On market since | Until |
|---|---|---|
| FrancePrimary placement | — | Still on market |
FR-MF-000003081The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.
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 →Certificate health across this manufacturer's portfolio.
39940SupplementedNotified 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.
View in glossary →No certificate specifically references this device's Basic UDI-DI.