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

Artiria Medical SA

Certificate G70DK 111736 0004

Rev. Rev. 01Amended
Valid until
Nov 11, 2030

Certificate G70DK 111736 0004 is a valid Technical documentation issued to Artiria Medical SA and registered in EUDAMED. Valid until November 11, 2030. View the full certificate record on MD Atlas.

Overview

Certificate number
G70DK 111736 0004
Certificate type
Technical documentation
Certificate status
Amended
Applicable legislation
MDR [Regulation (EU) 2017/745 on medical devices]
Version
1
Certificate ID
2443G70DK 111736 0004Rev. 01

Validity

Issued
Apr 10, 2026
Valid from
Apr 10, 2026
Valid until
Nov 11, 2030

Notified body

Notified body
TÜV SÜD Danmark
Notified body SRN
2443
Notified body country
Denmark

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

Status changes

  • Amended

Supersedes

  • G70DK 111736 0004IssuedNov 11, 2025 → Nov 10, 2030

Predecessor certificate not registered in EUDAMED.

Scope coverage

Unspecified1

1 scope

  • SmartGUIDE
    7649989542ASM-0001BD

Documents

LanguagesEN

Manufacturer

Manufacturer
Artiria Medical SA
Manufacturer SRN
CH-MF-000041617
Manufacturer country
Switzerland

Covered devices

  • SmartGUIDEClass III
    7649989542ASM-0001BD

Linked SSCPs

  • SSCP CLI-0029