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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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In Log S.A.S

Certificate G10 089173 0006

Rev. Rev. 00Issued
Valid until
Jul 12, 2028

Overview

Certificate number
G10 089173 0006
Certificate type
Quality management system
Certificate status
Issued
Applicable legislation
MDR [Regulation (EU) 2017/745 on medical devices]
Version
1
Certificate ID
0123G10 089173 0006Rev. 00

Validity

Issued
Jul 13, 2023
Valid from
Jul 13, 2023
Valid until
Jul 12, 2028

Manufacturer

Manufacturer
In Log S.A.S
Manufacturer SRN
FR-MF-000009507
Manufacturer country
France

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
Class IIb only

History

No status changes or preceding certificates are recorded.

Scope coverage

Class IIb1

1 scope

  • V92 - MEDICAL DEVICE SOFTWARE - NOT INCLUDED IN OTHER CLASSES
    Class IIb

Documents

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