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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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Neosyad SAS

Certificate M.2024.MDR.1051

Rev. 00Issued
Valid until
Oct 17, 2029

Overview

Certificate number
M.2024.MDR.1051
Certificate type
Quality management system
Certificate status
Issued
Applicable legislation
MDR [Regulation (EU) 2017/745 on medical devices]
Version
1
Certificate ID
2696M.2024.MDR.105100

Validity

Issued
Oct 18, 2024
Valid from
Oct 18, 2024
Valid until
Oct 17, 2029

Manufacturer

Manufacturer
Neosyad SAS
Manufacturer SRN
FR-MF-000037163
Manufacturer country
France

Notified body

Notified body
UDEM Adriatic d.o.o.
Notified body SRN
2696
Notified body country
Croatia

Covered devices

No specific devices are listed for this certificate.

Characteristics

Sterile
Yes
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
Yes
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

  • Lipofilling Device and Sterile Disposable Container Kit
    Class IIa

Documents

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