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

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

LimFlow SA

Certificate 1000261582

Rev. 01Issued
Valid until
Nov 27, 2028

Certificate 1000261582 is a valid Technical documentation issued to LimFlow SA and registered in EUDAMED. Valid until November 27, 2028. View the full certificate record on MD Atlas.

Overview

Certificate number
1000261582
Certificate type
Technical documentation
Certificate status
Issued
Applicable legislation
MDR [Regulation (EU) 2017/745 on medical devices]
Version
1
Certificate ID
0297100026158201

Validity

Issued
Aug 21, 2025
Valid from
Aug 21, 2025
Valid until
Nov 27, 2028

Notified body

Notified body
DQS Medizinprodukte GmbH
Notified body SRN
0297
Notified body country
Germany

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

Unspecified2

2 scopes

  • LimFlow Stent Graft System
    0850017630SGXDDLLLCE21XB
  • LimFlow Stent Graft System
    0850017630RGSDDLLLCE24RT

Documents

LanguagesEN

Manufacturer

Manufacturer
LimFlow SA
Manufacturer SRN
FR-MF-000011529
Manufacturer country
France

Covered devices

  • LimFlow Stent Graft SystemClass IIb
    0850017630SGXDDLLLCE21XB
  • LimFlow Stent Graft SystemClass IIb
    0850017630RGSDDLLLCE24RT

Linked SSCPs

  • SSCP LF-RA-OTH-33