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Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

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Bayer Consumer Care AG

Certificate G70 054972 0038

Rev. Rev. 01Issued
Valid until
Feb 17, 2030

Certificate G70 054972 0038 is a valid Technical documentation issued to Bayer Consumer Care AG and registered in EUDAMED. Valid until February 17, 2030. View the full certificate record on MD Atlas.

Overview

Certificate number
G70 054972 0038
Certificate type
Technical documentation
Certificate status
Issued
Applicable legislation
MDR [Regulation (EU) 2017/745 on medical devices]
Version
1
Certificate ID
0123G70 054972 0038Rev. 01

Validity

Issued
Jun 23, 2025
Valid from
Jun 23, 2025
Valid until
Feb 17, 2030

Manufacturer

Manufacturer
Bayer Consumer Care AG
Manufacturer SRN
CH-MF-000014141
Manufacturer country
Switzerland

Notified body

Notified body
TÜV SÜD Product Service GmbH
Notified body SRN
0123
Notified body country
Germany

Covered devices

  • Bepanthen Itch Relief Cream Class III
    4064273B161082100G5

Characteristics

Sterile
—
Human tissues
—
Animal tissues
—
In vitro diagnostics
—
Initial registration
Yes
New device
No
Discard allowed
No
SSCP enabled
Yes
Mechanism of scrutiny
No
Intended medical purpose
—
SPP applicable
—
Conditions applicable
No
MOS outside EUDAMED
—
QMS/MOS type
Others

History

No status changes or preceding certificates are recorded.

Scope coverage

Unspecified1

1 scope

  • Bepanthen Itch Relief Cream
    4064273B161082100G5

Documents

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