FITOFIX NEOPRENE ANKLE BRACE - M

Organization name

PHYTO PERFORMANCE ITALIA SRL

SRN

IT-MF-000008118

Manufacturer status

Active

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

• CW999

  Neoprene may cause allergic reactions of the skin. If rash develops discontinue use and consult a physician. In case of circulatory problems use it under medical supervision. Do not use it while sleeping.

Primary placement in Italy; available across 1 country total.

Trade name

FITOFIX NEOPRENE ANKLE BRACE - M

UDI-DI code

08031255008345

Basic UDI-DI

80312550009K4

Reference / catalog number

FX3001/M

Issuing entity

GS1

Risk category

Class I

Applicable legislation

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

Status

On the market

Quantity

1

Additional product description

This line includes a wide variety of excellent 4mm thickness bands studied for an active micro-massage pressure and an intense concentration of natural warmth on specific areas. fitofix improves articular and ligament performance during the sport activity thanks to a soft fabric on the skin and its 4-way stretch elasticity. Anatomic design, no-rub and flat stitch seams. Perfect fit, free of creases. The design of the outer fabric is very resistant and the inner lining in contact with the skin is very pleasant. Pressures on muscles and joints offer a better movement and a control sensation. Fits right or left ankle.

Additional information URL

No additional information URL provided by the manufacturer.

Clinical sizes

No clinical sizes registered for this device.

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

• Y090618LEG AND KNEE PROTECTIONS (INCLUDING SOCKS FOR AMPUTATED LEGS)