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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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BETATEX SPA

Certificate CVD001723

Rev. 00Issued
Valid until
Oct 23, 2027

Overview

Certificate number
CVD001723
Certificate type
Technical documentation
Certificate status
Issued
Applicable legislation
MDR [Regulation (EU) 2017/745 on medical devices]
Version
1
Certificate ID
0373CVD00172300

Validity

Issued
Nov 2, 2023
Valid from
Nov 2, 2023
Valid until
Oct 23, 2027

Manufacturer

Manufacturer
BETATEX SPA
Manufacturer SRN
IT-MF-000009955
Manufacturer country
Italy

Notified body

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

Covered devices

  • Lacci vascolari - Vascular loopsClass III
    805330078LVAGW

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

  • Lacci vascolari - Vascular loops
    805330078LVAGW

Documents

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