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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

MIG SPRAY — Class I MDD by VITROBIO SAS

MD Atlas
VITROBIO SAS

EUDAMED last updated this device on Apr 21, 2026

MIG SPRAY

B-VPFMIG-02MDD37

On the marketClass I

Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Organization name: VITROBIO SAS
UDI-DI code: D-VPFMIG-02MDD37
Reference / catalog number: VPF MIG - 02 MDD

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Manufacturer information

Organization name: VITROBIO SAS
SRN: FR-MF-000003081
Manufacturer status: Active

Critical warnings

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

CW032
EUDAMED did not publish a description for this code.
CW129
EUDAMED did not publish a description for this code.
CW275
EUDAMED did not publish a description for this code.
CW011
EUDAMED did not publish a description for this code.
CW010
EUDAMED did not publish a description for this code.
CW007
EUDAMED did not publish a description for this code.

Market distribution

Primary placement in France; available across 1 country total.

Country	On market since	Until
FrancePrimary placement		Still on market

Device identification

Trade name: MIG SPRAY
UDI-DI code: D-VPFMIG-02MDD37
Basic UDI-DI: B-VPFMIG-02MDD37
Reference / catalog number: VPF MIG - 02 MDD
Issuing entity: EUDAMED

Classification

Risk category: Class I
Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: Filmogen liquid bandage for the prevention of migraine
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: 2 pulvérisations / narine / 2-3 fois par jour

EMDN nomenclature code(s)

Q030199NASOPHARYNGEAL DEVICES - 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

This device is not currently linked to any other device.

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.