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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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Dermaroller GmbH

Certificate 6191GB449250723

Supplemented
Valid until
Sep 2, 2028

Certificate 6191GB449250723 is a valid Quality assurance issued to Dermaroller GmbH and registered in EUDAMED. Valid until September 2, 2028. View the full certificate record on MD Atlas.

Overview

Certificate number
6191GB449250723
Certificate type
Quality assurance
Certificate status
Supplemented
Applicable legislation
MDR [Regulation (EU) 2017/745 on medical devices]
Version
1
Certificate ID
04826191GB449250723

Validity

Issued
Jul 23, 2025
Valid from
Jul 23, 2025
Valid until
Sep 2, 2028

Notified body

Notified body
DNV MEDCERT GmbH
Notified body SRN
0482
Notified body country
Germany

Covered devices

No specific devices are listed for this certificate.

Characteristics

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

History

Status changes

  • Supplemented

Supersedes

  • 6191GB449240910IssuedSep 9, 2024 → Sep 1, 2028

Predecessor certificate not registered in EUDAMED.

Scope coverage

Class IIa2

2 scopes

  • MDA 0308 EMDN V901602
    Class IIa
  • MDN 1204 EMDN V901602
    Class IIa

Documents

LanguagesEN

Manufacturer

Manufacturer
Dermaroller GmbH
Manufacturer SRN
DE-MF-000005021
Manufacturer country
Germany