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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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  • MD Atlas
  • Documents

Bioland Technology Ltd.

Certificate V74 051313 0032

Rev. Rev. 00Issued
Valid until
Apr 16, 2030

Certificate V74 051313 0032 is a valid Technical documentation issued to Bioland Technology Ltd. and registered in EUDAMED. Valid until April 16, 2030. View the full certificate record on MD Atlas.

Overview

Certificate number
V74 051313 0032
Certificate type
Technical documentation
Certificate status
Issued
Applicable legislation
IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Version
1
Certificate ID
0123V74 051313 0032Rev. 00

Validity

Issued
Apr 17, 2025
Valid from
Apr 17, 2025
Valid until
Apr 16, 2030

Notified body

Notified body
TÜV SÜD Product Service GmbH
Notified body SRN
0123
Notified body country
Germany

Characteristics

Sterile
—
Human tissues
—
Animal tissues
—
In vitro diagnostics
—
Initial registration
Yes
New device
No
Discard allowed
No
SSCP enabled
Yes
Mechanism of scrutiny
No
Intended medical purpose
—
SPP applicable
—
Conditions applicable
No
MOS outside EUDAMED
—
QMS/MOS type
Others

History

No status changes or preceding certificates are recorded.

Scope coverage

Unspecified4

4 scopes

  • Blood Glucose Monitoring System
    6939184630021BK
  • Blood Glucose Meter
    6939184630001BD
  • Blood Glucose Test Strip
    6939184600001AC
  • Glucose control solution
    6939184650001C3

Documents

LanguagesEN

Manufacturer

Manufacturer
Bioland Technology Ltd.
Manufacturer SRN
CN-MF-000010625
Manufacturer country
China

Covered devices

  • Blood Glucose Monitoring SystemIVDR Class C
    6939184630021BK
  • Blood Glucose MeterIVDR Class C
    6939184630001BD
  • Blood Glucose Test StripIVDR Class C
    6939184600001AC
  • Glucose control solutionIVDR Class C
    6939184650001C3

Linked SSCPs

  • SSCP IVDR-BL-BGMS-21