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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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Noventure SL

Certificate CSQ0016230226

Rev. 02Amended
Valid until
Dec 21, 2028

Certificate CSQ0016230226 is a valid Quality management system issued to Noventure SL and registered in EUDAMED. Valid until December 21, 2028. View the full certificate record on MD Atlas.

Overview

Certificate number
CSQ0016230226
Certificate type
Quality management system
Certificate status
Amended
Applicable legislation
MDR [Regulation (EU) 2017/745 on medical devices]
Version
2
Certificate ID
0373CSQ001623022602

Validity

Issued
Feb 26, 2026
Valid from
Feb 26, 2026
Valid until
Dec 21, 2028

Notified body

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

Characteristics

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

History

Status changes

  • Amended

Supersedes

  • CSQ001623Quality management systemIssuedDec 22, 2023 → Dec 21, 2028

Scope coverage

Class III4

4 scopes

  • TASECTAN (capsules) GELENTERUM (capsules) NORMIA STOP (capsules)
    Class III
  • TASECTAN (sachets) GELENTERUM (sachets) NORMIA STOP (sachets)
    Class III
  • DEVICE
    Class III
  • DEVICE
    Class III

Documents

LanguagesENIT

Manufacturer

Manufacturer
Noventure SL
Manufacturer SRN
ES-MF-000000797
Manufacturer country
Spain

Covered devices

  • Tasectan capsulesClass III
    843659383TAS123LX
  • Tasectan sachetsClass III
    843659383TAS133M2