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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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synedra information technologies GmbH

Certificate 170780826

Rev. 170779401Withdrawn
Valid until
Dec 15, 2026

Overview

Certificate number
170780826
Certificate type
Technical documentation
Certificate status
Withdrawn
Applicable legislation
MDR [Regulation (EU) 2017/745 on medical devices]
Version
2
Certificate ID
0297170780826170779401

Validity

Issued
Jul 25, 2022
Valid from
Jul 25, 2022
Valid until
Dec 15, 2026

Manufacturer

Manufacturer
synedra information technologies GmbH
Manufacturer SRN
AT-MF-000000903
Manufacturer country
Austria

Notified body

Notified body
DQS Medizinprodukte GmbH
Notified body SRN
0297
Notified body country
Germany

Characteristics

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

History

Status changes

  • Withdrawn

Supersedes

  • 170780826Technical documentationIssuedJul 25, 2022 → Dec 15, 2026

Scope coverage

Unspecified2

2 scopes

  • synedra AIM
    912010070aimHG
  • synedra View Professional
    912010070viewproW6

Documents

LanguagesENDE

Covered devices

  • synedra AIMClass IIb
    912010070aimHG
  • synedra View ProfessionalClass IIb
    912010070viewproW6