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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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ЖИВАС ООД

Certificate 2025-MDR/QS-047

Rev. 0Issued
Valid until
Nov 10, 2028

Certificate 2025-MDR/QS-047 is a valid Quality management system issued to ЖИВАС ООД and registered in EUDAMED. Valid until November 10, 2028. View the full certificate record on MD Atlas.

Overview

Certificate number
2025-MDR/QS-047
Certificate type
Quality management system
Certificate status
Issued
Applicable legislation
MDR [Regulation (EU) 2017/745 on medical devices]
Version
1
Certificate ID
22652025-MDR/QS-0470

Validity

Issued
Sep 24, 2025
Valid from
Sep 24, 2025
Valid until
Nov 10, 2028

Manufacturer

Manufacturer
ЖИВАС ООД
Manufacturer SRN
BG-MF-000019745
Manufacturer country
Bulgaria

Notified body

Notified body
3EC International a.s.
Notified body SRN
2265
Notified body country
Slovakia

Covered devices

  • Septoquat AM MD/RFUClass IIb
    38002282401654

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
Yes
Intended medical purpose
No
SPP applicable
No
Conditions applicable
No
MOS outside EUDAMED
—
QMS/MOS type
Basic UDI-DI data and Class IIb

History

No status changes or preceding certificates are recorded.

Scope coverage

Class IIb2

2 scopes

  • Associated ammonium salts for the disinfection of medical devices
    Class IIb
  • DEVICE
    Class IIb

Documents

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