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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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Kangfu Medical Equipment Factory

Certificate 6131614CE01

Rev. Rev. 0Issued
Valid until
Nov 1, 2030

Certificate 6131614CE01 is a valid Quality assurance issued to Kangfu Medical Equipment Factory and registered in EUDAMED. Valid until November 1, 2030. View the full certificate record on MD Atlas.

Overview

Certificate number
6131614CE01
Certificate type
Quality assurance
Certificate status
Issued
Applicable legislation
MDR [Regulation (EU) 2017/745 on medical devices]
Version
1
Certificate ID
03446131614CE01Rev. 0

Validity

Issued
Nov 7, 2025
Valid from
Nov 7, 2025
Valid until
Nov 1, 2030

Notified body

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

Covered devices

No specific devices are listed for this certificate.

Characteristics

Sterile
No
Human tissues
No
Animal tissues
No
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 IIa1

1 scope

  • DEVICE
    Class IIa

Documents

LanguagesEN

Manufacturer

Manufacturer
Kangfu Medical Equipment Factory
Manufacturer SRN
CN-MF-000019108
Manufacturer country
China