EUALPLVN010P

Organization name

Nirial Pharma srl

SRN

IT-MF-000018760

Manufacturer status

Active

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

• CW277

  If you experience any adverse reactions, stop using the product immediately, consult your doctor and inform the manufacturer.
• CW032

  EUDAMED did not publish a description for this code.
• CW007

  Before use, check that the product is properly sealed and undamaged.
• CW135

  EUDAMED did not publish a description for this code.
• CW275

  If you are pregnant or breastfeeding, please consult your doctor first.
• CW999

  Wash your hands thoroughly before using the product. Do not use the product if you are known to be intolerant to even a single component of the formulation. Do not use the product if you have a confirmed hypersensitivity or allergy to one or more of its components. Do not touch the surface of the eye or any other surface with the tip of the bottle. Any serious incident occurring in connection with the device must be reported immediately to the Manufacturer and to the Competent Authority of the Member State in which the user and/or patient is established. Do not use the product for more than 30 consecutive days. Use in children must be supervised by an adult. Do not swallow. Product for external use. Ophthalmic product. No interactions with medicines are known. Other ophthalmic products (medicines or medical devices) must be used at least 15 minutes after instillation of these eye drops. Oral administration of other medical devices, medicines or supplements, in conjunction with these eye drops, must be carried out under the supervision of a doctor.
• CW010

  Please read the instructions for use.

Primary placement in Portugal; available across 1 country total.

Trade name

not provided

UDI-DI code

08052990632527

Basic UDI-DI

805299063OFTA001MA

Reference / catalog number

EUALPLVN010P

Issuing entity

GS1

Risk category

Class IIb

Applicable legislation

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

Status

On the market

Quantity

1

Additional product description

—

Additional information URL

No additional information URL provided by the manufacturer.

Clinical sizes

No clinical sizes registered for this device.

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

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

• Q02030299OPHTHALMOLOGY, LIQUID FLUIDS - OTHER