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

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phenox GmbH

Certificate 1000266808

Rev. 02Supplemented
Valid until
Dec 20, 2028

Certificate 1000266808 is a valid Technical documentation issued to phenox GmbH and registered in EUDAMED. Valid until December 20, 2028. View the full certificate record on MD Atlas.

Overview

Certificate number
1000266808
Certificate type
Technical documentation
Certificate status
Supplemented
Applicable legislation
MDR [Regulation (EU) 2017/745 on medical devices]
Version
1
Certificate ID
0297100026680802

Validity

Issued
Nov 20, 2025
Valid from
Nov 20, 2025
Valid until
Dec 20, 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

Status changes

  • Supplemented

Supersedes

  • 1000236360SupplementedAug 27, 2025 → Dec 19, 2028

Predecessor certificate not registered in EUDAMED.

Scope coverage

Unspecified1

1 scope

  • Device
    426012378FlowDiverterSV

Manufacturer

Manufacturer
phenox GmbH
Manufacturer SRN
DE-MF-000006524
Manufacturer country
Germany

Covered devices

  • 426012378FlowDiverterSVClass III
    426012378FlowDiverterSV

Linked SSCPs

  • SSCP 67.30.001_SSCP-FLOW DIVERTER

Documents

LanguagesDEEN