8602 / 8724

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

  EUDAMED did not publish a description for this code.
• CW011

  If you have diabetes, reduced sensitivity, skin disorders, circulatory or lymphatic disorders, or skin diseases, consult a doctor before use. Do not apply the bandage too tightly. Do not use the bandage in combination with other compression products, creams, oils, etc. If you experience tingling during use, or if the skin turns white or purple, remove the bandage immediately and check whether the correct size is being used. Do not use while sleeping or during extended periods of rest. Discontinue use and consult a doctor if symptoms persist.

Primary placement in Austria; available across 4 countries total.

Trade name

not provided

UDI-DI code

08712175941386

Basic UDI-DI

8712175_TD_11_SPSUPFS

Reference / catalog number

8602 / 8724

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

Achilles tendon bandage

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