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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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MD Atlas
Documents

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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