Горвидон (Gorvidon).

Organization name

Gofarm Sp. z o.o. Sp. k.

SRN

PL-MF-000003485

Manufacturer status

Active

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

• CW032

  EUDAMED did not publish a description for this code.
• CW999

  For reasons of hygiene and to avoid a possible transfer of infection it is recommended to use one product for one person. In order to maintain the properties of the product, do not manipulate the applicator (do not remove or unscrew). Do not apply the product lying down due to the risk of choking. If a patient is pregnant or breastfeeding, consult a physician or pharmacist before using this product. In the case of children over 3 years of age, the medical device should be used under the supervision of an adult. Avoid contact with the eyes. The product should not be used after the expiry date printed on the packaging and when the packaging is damaged. Do not use with other topical products. After applying the product on the irritated oral mucosa, a burning sensation may occur which should disappear on its own. If it lasts longer, consult your doctor.
• CW010

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

  EUDAMED did not publish a description for this code.

Primary placement in Poland; available across 1 country total.

Placed on the market in Poland; per-country availability dates not published.

Trade name

Горвидон (Gorvidon).

UDI-DI code

D-59037695023497V

Basic UDI-DI

B-59037695023497V

Reference / catalog number

ENT43

Issuing entity

EUDAMED

Risk category

Class I

Applicable legislation

MDD [Directive 93/42/EEC on medical devices]

Status

On the market

Quantity

1

Additional product description

Gorvidon is a medical device in the form of spray containing i.a. PVP (polyvinylpyrrolidone), tyndalized (non - viable) lactic acid bacteria Lacticaseibacillus rhamnosus, glycerin, xylitol, which covers mucous membrane of oral cavity and oropharynx creating protective film. Thanks to the moisturizing effect, it maintains the elasticity of the mucous membranes, which effectively soothes irritation and discomfort associated with dry mouth.

Additional information URL

No additional information URL provided by the manufacturer.

Clinical sizes

• 30 MU03

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

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

Certificate health across this manufacturer's portfolio.