Acandis GmbH

Certificate 1000308139

Rev. 02Supplemented

Valid until: Sep 18, 2029

Certificate 1000308139 is a valid Technical documentation issued to Acandis GmbH and registered in EUDAMED. Valid until September 18, 2029. View the full certificate record on MD Atlas.

Overview

Certificate number: 1000308139
Certificate type: Technical documentation
Certificate status: Supplemented
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Version: 1
Certificate ID: 0297100030813902

Validity

Issued: May 29, 2026
Valid from: May 29, 2026
Valid until: Sep 18, 2029

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

Status changes

Supplemented

Supersedes

1000302305SupplementedMar 16, 2026 → Sep 18, 2029

Predecessor certificate not registered in EUDAMED.

Scope coverage

Unspecified1

1 scope

ACCLINO flex plus Stent
426065033ACCLINOfpVV

Documents

LanguagesEN