6985

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, For sensory disorders of the skin, circulatory and lymphatic drainage disorders and skin diseases consult a doctor before use. Do not use the support in combination with other compression products, creams, skin oils, etc. In the event of tingling or numbness during the use remove the bandage immediately or loosen. Do not wear while sleeping or during prolonged resting periods. Discontinue use if skin irritation occurs and consult a doctor if this persists. Discontinue use if the elasticity of the bandage decreases. Inform the manufacturer and the competent authority about serious incidents. Store in the original packaging. This contains important information.

Primary placement in Netherlands; available across 1 country total.

Trade name

not provided

UDI-DI code

08710198301187

Basic UDI-DI

8712175_TD_11_BRACE57

Reference / catalog number

6985

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

Knee bandage, neoprene, OSFM

Additional information URL

No additional information URL provided by the manufacturer.

Clinical sizes

No clinical sizes registered for this device.

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

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

• M030499ELASTIC BANDAGES, SUPPORT AND COMPRESSION - OTHER