- Role
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EUDAMED update: Jan 28, 2026
DE-MF-000005504DE-MF-000005504SRN
An SRN is the unique EUDAMED identifier assigned to a manufacturer, authorised representative or importer when it registers as an actor.
View in glossary →SRN
An SRN is the unique EUDAMED identifier assigned to a manufacturer, authorised representative or importer when it registers as an actor.
View in glossary →Aesculap AG is a medical device manufacturer registered in EUDAMED. The company has 13,597 devices on the EU market across 27 countries. It holds 5 valid CE certificates. Headquartered in Tuttlingen , Germany. Explore the regulatory profile, devices and certificates on MD Atlas.
Devices placed in 27 countries
2 approved members
Certificate 20003GB450260622Manufacturer
Aesculap AG
Notified body
DNV MEDCERT GmbH
Version
1
Valid from
7/23/2026
Valid until
6/22/2031
Certificate G11 010066 0437Rev. Rev. 04Manufacturer
Aesculap AG
Notified body
TÜV SÜD Product Service GmbH
Version
1
Valid from
7/10/2025
Valid until
7/9/2030
Certificate G10 010066 0438Rev. Rev. 05Manufacturer
Aesculap AG
Notified body
TÜV SÜD Product Service GmbH
Version
1
Valid from
7/10/2025
Valid until
7/9/2030
Certificate 20333GB450240524Manufacturer
Aesculap AG
Notified body
DNV MEDCERT GmbH
Version
1
Valid from
5/24/2024
Valid until
5/23/2029
Certificate 20334GB450240524Manufacturer
Aesculap AG
Notified body
DNV MEDCERT GmbH
Version
1
Valid from
5/24/2024
Valid until
5/23/2029
Certificate G12 010066 0441Rev. Rev. 02Manufacturer
Aesculap AG
Notified body
TÜV SÜD Product Service GmbH
Version
1
Valid from
8/20/2024
Valid until
6/30/2026
Showing 1–25 of 13597 devices.
Showing 1–25 of 718 device families.
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