7948

Organization name

Bevaplast B.V.

SRN

NL-MF-000004386

Manufacturer status

Active

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

• CW011

  In case of sensitivity disorders of the skin, circulatory disorders or skin diseases, consult a doctor before use. Discontinue use if skin irritation occurs and consult a doctor if they persist or worsen. Keep out of the reach of children. Keep in the original packaging. It contains important information. Inform the manufacturer and the competent authority of any serious incidents.

Primary placement in Netherlands; available across 3 countries total.

Trade name

not provided

UDI-DI code

08712175937136

Basic UDI-DI

8712175_TD_13_FLEPA7W

Reference / catalog number

7948

Issuing entity

GS1

Risk category

Class I

Applicable legislation

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

Status

On the market

Quantity

6

Additional product description

75x115mm

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.

• M010203PADDING FELT

Certificate health across this manufacturer's portfolio.