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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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Med SSE System GmbH

Certificate DZ 1620448-1

Rev. Rev. 1Amended
Valid until
Sep 15, 2030

Certificate DZ 1620448-1 is a valid Quality assurance issued to Med SSE System GmbH and registered in EUDAMED. Valid until September 15, 2030. View the full certificate record on MD Atlas.

Overview

Certificate number
DZ 1620448-1
Certificate type
Quality assurance
Certificate status
Amended
Applicable legislation
MDR [Regulation (EU) 2017/745 on medical devices]
Version
3
Certificate ID
0197DZ 1620448-1Rev. 1

Validity

Issued
Feb 2, 2026
Valid from
Feb 2, 2026
Valid until
Sep 15, 2030

Notified body

Notified body
TÜV Rheinland LGA Products GmbH
Notified body SRN
0197
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
No
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
No
QMS/MOS type
Others

History

Status changes

  • Amended

Supersedes

  • DZ 1620448-1Quality assuranceIssuedSep 16, 2025 → Sep 15, 2030

Scope coverage

Class IIa1

1 scope

  • Products of Class lla: U070199 - INCONTINENCE-CONTROL, INTERNAL SYSTEMS - OTHERS
    Class IIa

Documents

LanguagesEN

Manufacturer

Manufacturer
Med SSE System GmbH
Manufacturer SRN
DE-MF-000008104
Manufacturer country
Germany