MIG SPRAY

Organization name

VITROBIO SAS

SRN

FR-MF-000003081

Manufacturer status

Active

10 warnings recorded — scroll inside the panel to see all entries.

• CW011

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• CW275

  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.
• CW010

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• CW007

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• CW129

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• CW135

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• CW416

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• CW262

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• CW036

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• CW018

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Primary placement in France; available across 1 country total.

Trade name

MIG SPRAY

UDI-DI code

03760076742576

Basic UDI-DI

376007674MIGSPRAY8M

Reference / catalog number

VPF MIG - 06 MDR

Issuing entity

GS1

Risk category

Class IIa

Applicable legislation

MDR [Regulation (EU) 2017/745 on medical devices]

Status

On the market

Quantity

1

Additional product description

Episodic migraine prevention with or without aura

Additional information URL

No additional information URL provided by the manufacturer.

Clinical sizes

• 2 pulvérisations / narine / 3 fois par jour

• Batch number
• Expiration date
• Manufacturing date
• Serial number
• Software identification

European Medical Device Nomenclature — the EU product classification assigned to this device.

• Q030199NASOPHARYNGEAL DEVICES - OTHER