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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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UROMED Kurt Drews KG

Certificate 20561GB450250724

Issued
Valid until
Jul 23, 2030

Overview

Certificate number
20561GB450250724
Certificate type
Technical documentation
Certificate status
Issued
Applicable legislation
MDR [Regulation (EU) 2017/745 on medical devices]
Version
1
Certificate ID
048220561GB450250724

Validity

Issued
Jul 24, 2025
Valid from
Jul 24, 2025
Valid until
Jul 23, 2030

Manufacturer

Manufacturer
UROMED Kurt Drews KG
Manufacturer SRN
DE-MF-000006084
Manufacturer country
Germany

Notified body

Notified body
DNV MEDCERT GmbH
Notified body SRN
0482
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

No status changes or preceding certificates are recorded.

Scope coverage

Unspecified4

4 scopes

  • US01
    04250098810055ET
  • US01
    04250098810056EV
  • US01
    04250098810057EX
  • US01
    04250098810058EZ

Documents

LanguagesEN

Covered devices

  • US01Class IIb
    04250098810055ET
  • US01Class IIb
    04250098810056EV
  • US01Class IIb
    04250098810057EX
  • US01Class IIb
    04250098810058EZ