EUDAMED last updated this device on Jul 21, 2026

Floragyn Lavanda

B-08058333980942

On the marketClass IIb

Applicable legislation: —
Organization name: SO.SE.PHARM S.R.L. SOCIETA' DI SERVIZIO PER L'INDUSTRIA FARMACEUT ICA ED AFFINI
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 →: 08058333980942
Reference / catalog number: 700

Regulatory classification unavailableThis product's Basic UDI record hasn't been published in EUDAMED yet. Classification and compliance details will appear automatically once EUDAMED publishes it.

Floragyn Lavanda is an EU-regulated medical device registered in EUDAMED. It is classified as Class IIb. Manufactured by SO.SE.PHARM S.R.L. SOCIETA' DI SERVIZIO PER L'INDUSTRIA FARMACEUT ICA ED AFFINI. Placed on the EU market in Italy. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.

Device identification

Trade name: Floragyn Lavanda
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 →: 08058333980942
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 →: B-08058333980942
Reference / catalog number: 700
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 →: GS1

Classification

Risk category: Class IIb
Applicable legislation: —
Status: On the market

Device details

Quantity: 1
Additional product description: Floragyn Lavanda : 5 lavande monouso da 140 ml
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

UDI-DI DataMatrix

Encoded

(01)08058333980942

EMDN nomenclature code(s)

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

U089009VAGINAL APPLICATORS, SINGLE-USE

Critical warnings

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

Consult instructions for use
Do not re-use
Do not use past indicated date
Do not use if package is damaged
Ask your pharmacist or doctor for advice before using or taking the product (e.g. if pregnant or breastfeeding)

Compliance flags

Safety

Direct marking

Regulatory

Sterilization

Lifecycle

New device

Market distribution

Primary placement in Italy; available across 1 country total.

Country	On market since	Until
ItalyPrimary placement	—	Still on market

Floragyn Lavanda

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Device details

UDI-PI traceability

UDI-DI DataMatrix

EMDN nomenclature code(s)

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Safety

Regulatory

Lifecycle

Market distribution

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Device identification

Classification

Device details

Manufacturer information

UDI-PI traceability

UDI-DI DataMatrix

EMDN nomenclature code(s)

Critical warnings

Compliance flags

Safety

Regulatory

Lifecycle

Certificates

Legacy certificates

Certificates covering this device

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Manufacturer information

Certificates covering this device

Certificates

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