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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

Rinopanteina Plus — Class IIa MDD by Drugs Minerals and…

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

EUDAMED last updated this device on Jul 28, 2025

Rinopanteina Plus

B-ITMF24945GR090VXM

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-ITMF24945GR090VXM
Reference / catalog number: GR090V

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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

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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 Cyprus; available across 2 countries total.

Country	On market since	Until
CyprusPrimary placement	Jul 22, 2018	Dec 31, 2028
EL	Jul 22, 2018	Dec 31, 2028

Device identification

Trade name: Rinopanteina Plus
UDI-DI code: D-ITMF24945GR090VXM
Basic UDI-DI: B-ITMF24945GR090VXM
Reference / catalog number: GR090V
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

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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