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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 Ltd

Certificate 2245542TD01

Rev. Rev. 1Issued
Valid until
Feb 1, 2029

Certificate 2245542TD01 is a valid Technical documentation issued to phenox Ltd and registered in EUDAMED. Valid until February 1, 2029. View the full certificate record on MD Atlas.

Overview

Certificate number
2245542TD01
Certificate type
Technical documentation
Certificate status
Issued
Applicable legislation
MDR [Regulation (EU) 2017/745 on medical devices]
Version
1
Certificate ID
03442245542TD01Rev. 1

Validity

Issued
Jul 5, 2024
Valid from
Jul 5, 2024
Valid until
Feb 1, 2029

Manufacturer

Manufacturer
phenox Ltd
Manufacturer SRN
IE-MF-000011333
Manufacturer country
Ireland

Notified body

Notified body
DEKRA Certification B.V.
Notified body SRN
0344
Notified body country
Netherlands

Covered devices

  • pNOVUS 21 MicrocatheterClass III
    539153091pNOVUSFAMILYYK

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

Unspecified1

1 scope

  • pNOVUS 21 Microcatheter
    539153091pNOVUSFAMILYYK

Documents

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