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

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

Occlutech GmbH

Certificate 51030-61-B0

Rev. Rev. 0Issued
Valid until
Jun 28, 2028

Certificate 51030-61-B0 is a valid Technical documentation issued to Occlutech GmbH and registered in EUDAMED. Valid until June 28, 2028. View the full certificate record on MD Atlas.

Overview

Certificate number
51030-61-B0
Certificate type
Technical documentation
Certificate status
Issued
Applicable legislation
MDR [Regulation (EU) 2017/745 on medical devices]
Version
1
Certificate ID
012451030-61-B0Rev. 0

Validity

Issued
Jun 29, 2023
Valid from
Jun 29, 2023
Valid until
Jun 28, 2028

Manufacturer

Manufacturer
Occlutech GmbH
Manufacturer SRN
DE-MF-000005104
Manufacturer country
Germany

Notified body

Notified body
DEKRA Certification GmbH
Notified body SRN
0124
Notified body country
Germany

Covered devices

  • Occlutech Occlusions PusherClass III
    426018252OOPFL

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

  • Occlutech Occlusions Pusher
    426018252OOPFL

Documents

LanguagesEN