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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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livetec Ingenieurbüro GmbH

Certificate HZ 1448989-1

Rev. Rev. 0Issued
Valid until
Oct 13, 2030

Overview

Certificate number
HZ 1448989-1
Certificate type
Quality management system
Certificate status
Issued
Applicable legislation
MDR [Regulation (EU) 2017/745 on medical devices]
Version
1
Certificate ID
0197HZ 1448989-1Rev. 0

Validity

Issued
Oct 14, 2025
Valid from
Oct 14, 2025
Valid until
Oct 13, 2030

Manufacturer

Manufacturer
livetec Ingenieurbüro GmbH
Manufacturer SRN
DE-MF-000005598
Manufacturer country
Germany

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
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 IIb1

1 scope

  • Z120615 – Therapeutic Lasers
    Class IIb

Documents

LanguagesEN