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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

A-Vita Hydra + — Class IIa MDD by Drugs Minerals and…

MD Atlas
Drugs Minerals and Generics Italia S.r.l.

EUDAMED last updated this device on Dec 23, 2025

A-Vita Hydra +

B-ITMF24945FI235V-01E2

On the marketClass IIa

Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Organization name: Drugs Minerals and Generics Italia S.r.l.
UDI-DI code: D-ITMF24945FI235V-01E2
Reference / catalog number: FI235V-01

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View device family (Basic UDI)

Manufacturer information

Organization name: Drugs Minerals and Generics Italia S.r.l.
SRN: IT-MF-000024945
Manufacturer status: Active

Related devices

FI080VM803412518TF046SOn the market A-Vita PlusB-ITMF24945FI081V-01DMOn the market FI085VM803412518TF036QOn the market A-VITA PLUS (Gocce Nasali)B-ITMF24945FI080VTYOn the market A-VITA PLUS (Unguento Nasale)B-ITMF24945FI085VUFOn the market

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.

Critical warnings

1 warning recorded — scroll inside the panel to see all entries.

CW999
Do not use this product in case of known hypersensitivity to any component of the product

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Market distribution

Primary placement in Finland; available across 1 country total.

Country	On market since	Until
FinlandPrimary placement	Dec 12, 2018	Dec 31, 2028

Device identification

Trade name: A-Vita Hydra +
UDI-DI code: D-ITMF24945FI235V-01E2
Basic UDI-DI: B-ITMF24945FI235V-01E2
Reference / catalog number: FI235V-01
Issuing entity: EUDAMED

Classification

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

Device details

Quantity: 1
Additional product description: Variante 2
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

D-ITMF24945FI235V-01E2

DataMatrix generation currently supports GS1-issued UDIs. HIBCC / ICCBBA support is coming.

EMDN nomenclature code(s)

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

M9002PROTECTIVE DEVICES, LUBRICANTS AND SOOTHING DEVICES (SPRAYS, GELS, FLUIDS AND CREAMS)

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

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