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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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Clinomic Medical GmbH

Certificate G10 110050 0002

Rev. Rev. 00Issued
Valid until
Jan 25, 2028

Certificate G10 110050 0002 is a valid Quality management system issued to Clinomic Medical GmbH and registered in EUDAMED. Valid until January 25, 2028. View the full certificate record on MD Atlas.

Overview

Certificate number
G10 110050 0002
Certificate type
Quality management system
Certificate status
Issued
Applicable legislation
MDR [Regulation (EU) 2017/745 on medical devices]
Version
1
Certificate ID
0123G10 110050 0002Rev. 00

Validity

Issued
Jan 26, 2023
Valid from
Jan 26, 2023
Valid until
Jan 25, 2028

Notified body

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

Covered devices

No specific devices are listed for this certificate.

Characteristics

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

History

No status changes or preceding certificates are recorded.

Scope coverage

Class IIa1

1 scope

  • Z12030201 - CENTRAL INFORMATION COMPUTING SYSTEMS
    Class IIa

Documents

LanguagesEN

Manufacturer

Manufacturer
Clinomic Medical GmbH
Manufacturer SRN
DE-MF-000013339
Manufacturer country
Germany