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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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SIFI S.p.A.

Certificate CVD0015230125

Rev. 01Issued
Valid until
Sep 21, 2028

Overview

Certificate number
CVD0015230125
Certificate type
Technical documentation
Certificate status
Issued
Applicable legislation
MDR [Regulation (EU) 2017/745 on medical devices]
Version
1
Certificate ID
0373CVD001523012501

Validity

Issued
Jan 9, 2025
Valid from
Jan 9, 2025
Valid until
Sep 21, 2028

Manufacturer

Manufacturer
SIFI S.p.A.
Manufacturer SRN
IT-MF-000020853
Manufacturer country
Italy

Notified body

Notified body
ISTITUTO SUPERIORE DI SANITA'
Notified body SRN
0373
Notified body country
Italy

Covered devices

  • SF 104-XNT/ATSClass III
    8027864SIFIMDF28NH

Characteristics

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

History

No status changes or preceding certificates are recorded.

Scope coverage

Unspecified1

1 scope

  • SF 104-XNT/ATS
    8027864SIFIMDF28NH

Documents

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