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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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terraplasma medical GmbH

Certificate HZ 1380540-1

Rev. Rev. 0Issued
Valid until
Nov 12, 2029

Certificate HZ 1380540-1 is a valid Quality management system issued to terraplasma medical GmbH and registered in EUDAMED. Valid until November 12, 2029. View the full certificate record on MD Atlas.

Overview

Certificate number
HZ 1380540-1
Certificate type
Quality management system
Certificate status
Issued
Applicable legislation
MDR [Regulation (EU) 2017/745 on medical devices]
Version
1
Certificate ID
0197HZ 1380540-1Rev. 0

Validity

Issued
Nov 13, 2024
Valid from
Nov 13, 2024
Valid until
Nov 12, 2029

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
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

No status changes or preceding certificates are recorded.

Scope coverage

Class IIa1

1 scope

  • Z120190 - VARIOUS INSTRUMENTS FOR GENERAL AND MULTIDISCIPLINARY SURGERY
    Class IIa

Documents

LanguagesEN

Manufacturer

Manufacturer
terraplasma medical GmbH
Manufacturer SRN
DE-MF-000011250
Manufacturer country
Germany