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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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UAB Teltonika Telemedic

Certificate MDR-009

Rev. 1Issued
Valid until
Mar 19, 2029

Certificate MDR-009 is a valid Quality management system issued to UAB Teltonika Telemedic and registered in EUDAMED. Valid until March 19, 2029. View the full certificate record on MD Atlas.

Overview

Certificate number
MDR-009
Certificate type
Quality management system
Certificate status
Issued
Applicable legislation
MDR [Regulation (EU) 2017/745 on medical devices]
Version
1
Certificate ID
1304MDR-0091

Validity

Issued
Mar 20, 2024
Valid from
Mar 21, 2024
Valid until
Mar 19, 2029

Notified body

Notified body
SLOVENIAN INSTITUTE OF QUALITY AND METROLOGY - SIQ
Notified body SRN
1304
Notified body country
Slovenia

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 IIa2

2 scopes

  • VITAL SIGNS TELEMETRY INSTRUMENTS - MEDICAL DEVICE SOFTWARE
    Class IIa
  • MyHealth App
    Class IIa

Documents

LanguagesEN

Manufacturer

Manufacturer
UAB Teltonika Telemedic
Manufacturer SRN
LT-MF-000007642
Manufacturer country
Lithuania