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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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Eufoton Srl

Certificate ITD 1024592 1

Rev. 1.0Issued
Valid until
May 15, 2029

Overview

Certificate number
ITD 1024592 1
Certificate type
Quality assurance
Certificate status
Issued
Applicable legislation
MDR [Regulation (EU) 2017/745 on medical devices]
Version
1
Certificate ID
1936ITD 1024592 11.0

Validity

Issued
Feb 24, 2025
Valid from
Feb 24, 2025
Valid until
May 15, 2029

Manufacturer

Manufacturer
Eufoton Srl
Manufacturer SRN
IT-MF-000009227
Manufacturer country
Italy

Notified body

Notified body
TUV Rheinland Italia SRL
Notified body SRN
1936
Notified body country
Italy

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
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

  • MDN 1208 Non-active non-implantable instruments MDN 1208 Strumenti non impiantabili non attivi
    Class IIa

Documents

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