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

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

P+F Products and Features GmbH

Certificate 1434-MDR-002/2026

Rev. 1/05.02.2026/S/090/BM/2023Issued
Valid until
Feb 5, 2031

Certificate 1434-MDR-002/2026 is a valid Quality management system issued to P+F Products and Features GmbH and registered in EUDAMED. Valid until February 5, 2031. View the full certificate record on MD Atlas.

Overview

Certificate number
1434-MDR-002/2026
Certificate type
Quality management system
Certificate status
Issued
Applicable legislation
MDR [Regulation (EU) 2017/745 on medical devices]
Version
1
Certificate ID
14341434-MDR-002/20261/05.02.2026/S/090/BM/2023

Validity

Issued
Feb 5, 2026
Valid from
Feb 5, 2026
Valid until
Feb 5, 2031

Notified body

Notified body
POLSKIE CENTRUM BADAN I CERTYFIKACJI S.A.
Notified body SRN
1434
Notified body country
Poland

Covered devices

No specific devices are listed for this certificate.

Characteristics

Sterile
Yes
Human tissues
No
Animal tissues
Yes
In vitro diagnostics
No
Initial registration
Yes
New device
No
Discard allowed
No
SSCP enabled
No
Mechanism of scrutiny
No
Intended medical purpose
No
SPP applicable
No
Conditions applicable
No
MOS outside EUDAMED
—
QMS/MOS type
Others

History

No status changes or preceding certificates are recorded.

Scope coverage

Class III2

2 scopes

  • P07030104 - BIOLOGICAL VALVES, BICAVAL
    Class III
  • TricValve® Transcatheter Bicaval Valve System
    Class III

Documents

LanguagesEN

Manufacturer

Manufacturer
P+F Products and Features GmbH
Manufacturer SRN
DE-MF-000008580
Manufacturer country
Germany