MD Atlas
BlogPricingSign in
MD Atlas
Made In Tracker
Made In TrackerEasyUDI
Legal
Privacy PolicyLegal Notice
About
AboutFAQGlossaryBlogMCP serverPartnersContact

Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

Subscribe to our monthly newsletter:

  • MD Atlas
  • Documents

Lifestream Pharma N.V.

Certificate BE23/00000293

Rev. 2Supplemented
Valid until
Oct 3, 2028

Certificate BE23/00000293 is a valid Quality management system issued to Lifestream Pharma N.V. and registered in EUDAMED. Valid until October 3, 2028. View the full certificate record on MD Atlas.

Overview

Certificate number
BE23/00000293
Certificate type
Quality management system
Certificate status
Supplemented
Applicable legislation
MDR [Regulation (EU) 2017/745 on medical devices]
Version
2
Certificate ID
1639BE23/000002932

Validity

Issued
Nov 25, 2025
Valid from
Nov 25, 2025
Valid until
Oct 3, 2028

Notified body

Notified body
SGS Belgium NV
Notified body SRN
1639
Notified body country
Belgium

Characteristics

Sterile
No
Human tissues
No
Animal tissues
No
In vitro diagnostics
No
Initial registration
No
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
No
QMS/MOS type
Basic UDI-DI data only

History

Status changes

  • Supplemented

Supersedes

  • BE23/00000293Quality management systemIssuedOct 3, 2023 → Oct 3, 2028

Scope coverage

Class IIa4

4 scopes

  • MDN1213, MDS1008
    Class IIa
  • DEVICE
    Class IIa
  • DEVICE
    Class IIa
  • DEVICE
    Class IIa

Documents

LanguagesEN

Manufacturer

Manufacturer
Lifestream Pharma N.V.
Manufacturer SRN
BE-MF-000001909
Manufacturer country
Belgium

Covered devices

  • bioXtra Dry Mouth Class IIa
    542500512BXMR01ZQ
  • bioXtra Dry Mouth Class IIa
    542500512BXMS01ZV
  • bioXtra Dry Mouth Class IIa
    542500512BXOG01YF