Hyalocid Vaginal Gel

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.

• CW010

  EUDAMED did not publish a description for this code.
• CW009

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

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

  Hypersensitivity (allergy) to product ingredients. Chronic and acute inflammation, manifested by purulent discharge or excessive mucus discharge, requiring the advice of a gynecologist. Vaginal product, avoid contact with eyes. Do not use simultaneously with other vaginal preparations (including vaginal contraceptives). Do not use during menstruation or in the case of increased vaginal discharge. In case of any doubt or the feeling of burning or itching, discontinue use of the product and consult with your doctor, or other qualified health care professional. During pregnancy, the preparation can be used only as prescribed by the doctor.

Primary placement in Poland; available across 1 country total.

Trade name

Hyalocid Vaginal Gel

UDI-DI code

D-6297001028100X7

Basic UDI-DI

B-6297001028100X7

Reference / catalog number

WH01

Issuing entity

EUDAMED

Risk category

Class IIb

Applicable legislation

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

Status

On the market

Quantity

1

Additional product description

Hyalocid Vaginal gel is a delicate, colorless and odorless Hyalocid Vaginal gel that protects tissues and restores the natural physiological state of the vaginal mucosa after gynecological surgery. Due to the moisturizing effect and ensuring the appropriate pH, it soothes the symptoms of vaginal atrophy such as itching, burning, redness, swelling, abnormal discharge, the feeling of tissue tension or discomfort during sexual intercourse. Due to proper hydration, an appropriate environment is created for the natural regeneration processes to take place.

Additional information URL

No additional information URL provided by the manufacturer.

Clinical sizes

• 5 MU48

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.