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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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MCM Klosterfrau Vertriebs GmbH

Certificate G10 005567 0005

Rev. Rev. 00Issued
Valid until
Nov 27, 2029

Overview

Certificate number
G10 005567 0005
Certificate type
Quality management system
Certificate status
Issued
Applicable legislation
MDR [Regulation (EU) 2017/745 on medical devices]
Version
1
Certificate ID
0123G10 005567 0005Rev. 00

Validity

Issued
Nov 28, 2024
Valid from
Nov 28, 2024
Valid until
Nov 27, 2029

Manufacturer

Manufacturer
MCM Klosterfrau Vertriebs GmbH
Manufacturer SRN
DE-MF-000006191
Manufacturer country
Germany

Notified body

Notified body
TÜV SÜD Product Service GmbH
Notified body SRN
0123
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
Yes
Intended medical purpose
No
SPP applicable
No
Conditions applicable
No
MOS outside EUDAMED
—
QMS/MOS type
Class IIb only

History

No status changes or preceding certificates are recorded.

Scope coverage

Class IIb6

6 scopes

  • G0499 - ORALLY ADMINISTERED GASTROINTESTINAL DEVICES - OTHER
    Class IIb
  • G0499 - ORALLY ADMINISTERED GASTROINTESTINAL DEVICES - OTHER
    Class IIb
  • Q0399 - ENT DEVICES - OTHER
    Class IIb
  • Q0399 - ENT DEVICES - OTHER
    Class IIb
  • Q0399 - ENT DEVICES - OTHER
    Class IIb
  • Q0399 - ENT DEVICES - OTHER
    Class IIb

Documents

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