Noventure S.L.U.

Certificate MDR 00064-B

Rev. 2Issued

Valid until: Nov 14, 2029

Certificate MDR 00064-B is a valid Technical documentation issued to Noventure S.L.U. and registered in EUDAMED. Valid until November 14, 2029. View the full certificate record on MD Atlas.

Overview

Certificate number: MDR 00064-B
Certificate type: Technical documentation
Certificate status: Issued
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Version: 1
Certificate ID: 0476MDR 00064-B2

Validity

Issued: Mar 27, 2025
Valid from: Mar 27, 2025
Valid until: Nov 14, 2029

Notified body

Notified body: KIWA CERMET ITALIA S.P.A.
Notified body SRN: 0476
Notified body country: Italy

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

Unspecified6

6 scopes

XILAPLUS AF capsules
843659383XIA623N6
Xilaplus AF sachets with flavour
843659383XIA633N9
XILAPLUS AF sachets without flavour
843659383XIA643NC
Xilaplus AF tablets
843659383XIA653NF
UTIPRO PLUS AF capsules
843659383UTA423QE
Utipro Plus AF tablets
843659383UTA433QH