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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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DMG Chemisch-Pharmazeutische Fabrik GmbH

Certificate 0302GB448240604

Issued
Valid until
Dec 21, 2027

Overview

Certificate number
0302GB448240604
Certificate type
Quality management system
Certificate status
Issued
Applicable legislation
MDR [Regulation (EU) 2017/745 on medical devices]
Version
1
Certificate ID
04820302GB448240604

Validity

Issued
Jun 4, 2024
Valid from
Jun 4, 2024
Valid until
Dec 21, 2027

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
No
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

No status changes or preceding certificates are recorded.

Scope coverage

Class IIa8

8 scopes

  • MDN 1103 EMDN Q0101
    Class IIa
  • MDN 1103 EMDN Q0102
    Class IIa
  • MDN 1103 EMDN Q0190
    Class IIa
  • MDN 1209 EMDN Q0101
    Class IIa
  • MDN 1209 EMDN Q0102
    Class IIa
  • MDN 1209 EMDN Q0105
    Class IIa
  • MDN 1209 EMDN Q0106
    Class IIa
  • MDN 1209 EMDN Q0199
    Class IIa

Documents

LanguagesEN

Manufacturer

Manufacturer
DMG Chemisch-Pharmazeutische Fabrik GmbH
Manufacturer SRN
DE-MF-000006027
Manufacturer country
Germany