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Atlas

by İnvamed Sağlik İlaç Sanayi̇ Ve Ti̇caret A.Ş. Türkiye EUDAMED

Ref AESG-7-23

EMDN P0704020202

Regulatory status

as of 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-8683498158419GD Basic UDI-DIDate17 Nov 2023RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Expiring (legacy directive)
  • Not covered

European Union — CE/MDD Expiring (legacy directive)

Certificates: none listed in EUDAMED

Specification

EUDAMED · synced 23 Oct 2026

Device Name
Atlas Endovascular Stent Graft System 7.0 x 23
Model / Reference
AESG-7-23
Primary DI / UDI-DI
D-8683498158419GD
Basic UDI-DI
B-8683498158419GD
EMDN Code
P0704020202 Peripheral vascular coated stents
Device Class
Class IIb
Market of Registration
Türkiye

Manufacturer details

EUDAMED SRN
TR-MF-000019963

Other devices from İnvamed Sağlik İlaç Sanayi̇ Ve Ti̇caret A.Ş.

See all devices from İnvamed Sağlik İlaç Sanayi̇ Ve Ti̇caret A.Ş. →

Properties & raw data

Show properties, registry sources and raw records
  • Sterile
  • Implantable
Other properties (9)
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No

Sources (1)

  • EUDAMED d800089a-170e-4b3c-bf7b-2705a0cf9c95 61 fields · synced 23 Oct 2026