Previs S.r.l.

Certificate 0425-MDR-030043-01

Rev. 01Issued

Valid until: Oct 1, 2028

Certificate 0425-MDR-030043-01 is a valid Quality assurance issued to Previs S.r.l. and registered in EUDAMED. Valid until October 1, 2028. View the full certificate record on MD Atlas.

Overview

Certificate number: 0425-MDR-030043-01
Certificate type: Quality assurance
Certificate status: Issued
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Version: 1
Certificate ID: 04250425-MDR-030043-0101

Validity

Issued: Oct 2, 2023
Valid from: Oct 2, 2023
Valid until: Oct 1, 2028

Notified body

Notified body: ICIM S.P.A.
Notified body SRN: 0425
Notified body country: Italy

Covered devices

No specific devices are listed for this certificate.

Characteristics

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

History

No status changes or preceding certificates are recorded.

Scope coverage

Class IIa2

2 scopes

BENDE CON OSSIDO DI ZINCO "PREVIZINC A - E- EC" / ZINC OXIDE BANDAGES "PREVIZINC A - E- EC"
Class IIa
PREVIZINC A, PREVIZINC E, PREVIZINC EC
Class IIa