BLIZNOXIN Scar gel 20ml tube in a carton with instructions for use. Polish language version.

Organization name

LABORATOIRE L'IDEAL Parisien Sp. z o.o.

SRN

PL-MF-000005402

Manufacturer status

Active

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

• CW999

  Do not use if you are allergic to the product's ingredients If you experience itching or stinging after using the product, this may mean you are allergic to the product's ingredients; in that case, STOP USING THE PRODUCT. Avoid accidental contact with the mucous membrane of eyes and mucous membranes Do not use on damaged skin or unhealed wounds. Do not use other products directly after applying the gel to the scar. Keep away from children. Do not use after expiration date. Do not use if the packaging is damaged or tampered with before first opening The use of silicone gel can cause an MRI artifact to appear and be confused with a metallic foreign body. This warning should be given to MRI professionals. The product is intended for external use only on undamaged skin

Primary placement in Poland; available across 1 country total.

Trade name

not provided

UDI-DI code

05908226260664

Basic UDI-DI

B-05908226260664

Reference / catalog number

BLIZNOXIN Scar gel 20ml tube in a carton with instructions for use. Polish language version.

Issuing entity

GS1

Risk category

Class I

Applicable legislation

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

Status

On the market

Quantity

1

Additional product description

Advanced medical aid used for the treatment of previously healed scars of different origins. The gel has a smoothing and soothing effect on scar tissue, improves its appearance by softening and evening out the colour, and reducing the discoloration. The product reduces itching and the tangible tension of the skin. The product is recommended for: 1) enhancing the treatment of scars of various origins, including after: - burns, - injuries (abrasions, cuts), - surgeries (C-section), - surgical treatment - acne 2) as the scar's protective layer against rubbing and sunlight

Additional information URL

https://www.lideal.pl/

Clinical sizes

• 20 MU03

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

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

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