8545 / 8742

Organization name

Bevaplast B.V.

SRN

NL-MF-000004386

Manufacturer status

Active

Certificate health across this manufacturer's portfolio.

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

• CW010

  ISO symbol
• CW011

  ISO symbol, In the case of sensory disorders of the skin, circulatory and lymphatic drainage disorders as well as skin formations consult a doctor before use. Do not use the knee ligament in combination with other compression products, creams, skin oils, etc. In the event of tingling or numbness during the use, or white or violet colouring of the skin, remove the bandage immediately and check whether the correct size bandage is worn. Do not wear while sleeping or during longer rest periods. Stop using in case skin irritations occur and consult a doctor if the symptoms persists. Discontinue use if if the elasticity of the bandage decreases. Keep out of reach of children. Inform the manufacturer and the relevant authorities about any serious incidents. Store in the original packaging, which contains important information.

Primary placement in Netherlands; available across 5 countries total.

Trade name

not provided

UDI-DI code

08712175940488

Basic UDI-DI

8712175_TD_11_SPSUPFS

Reference / catalog number

8545 / 8742

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

Bandage kee with copper, size M

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.

• M030499ELASTIC BANDAGES, SUPPORT AND COMPRESSION - OTHER