Bepanthen® SensiCalm

Organization name

Bayer Consumer Care AG

SRN

CH-MF-000014141

Manufacturer status

Active

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

• CW010

  EUDAMED did not publish a description for this code.
• CW264

  EUDAMED did not publish a description for this code.
• CW999

  Do not use in the case of known allergies to any listed ingredient. If an allergic reaction develops, you should stop using the product. If you experience any skin reaction, discontinue use and seek medical advice if necessary. For external use only. Keep out of reach and sight of children. Choking hazard may occur with the tube cap. The product should only be used before the expiry date stated on the box. In case of direct contact with the eyes, rinse thoroughly with clean water.

Primary placement in France; available across 3 countries total.

Trade name

Bepanthen® SensiCalm

UDI-DI code

04064273150172

Basic UDI-DI

4064273B161082100G5

Reference / catalog number

04064273150172

Issuing entity

GS1

Risk category

Class III

Applicable legislation

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

Status

On the market

Quantity

1

Additional product description

—

Additional information URL

No additional information URL provided by the manufacturer.

Clinical sizes

No clinical sizes registered for this device.

• M04041503DRESSINGS IN SOLUTIONS, EMULSIONS, GELS, POWDERS WITH SYNTHETIC COMPONENTS

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

Certificate health across this manufacturer's portfolio.