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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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Cupid Limited

Certificate 2025-IVDR/TD-009

Rev. 00Issued
Valid until
Oct 13, 2030

Certificate 2025-IVDR/TD-009 is a valid Technical documentation issued to Cupid Limited and registered in EUDAMED. Valid until October 13, 2030. View the full certificate record on MD Atlas.

Overview

Certificate number
2025-IVDR/TD-009
Certificate type
Technical documentation
Certificate status
Issued
Applicable legislation
IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Version
1
Certificate ID
22652025-IVDR/TD-00900

Validity

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

Notified body

Notified body
3EC International a.s.
Notified body SRN
2265
Notified body country
Slovakia

Characteristics

Sterile
—
Human tissues
—
Animal tissues
—
In vitro diagnostics
—
Initial registration
Yes
New device
No
Discard allowed
No
SSCP enabled
No
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

Unspecified1

1 scope

  • Pregnancy hCG Test Kit
    890600528cuphcgKG

Documents

LanguagesEN

Manufacturer

Manufacturer
Cupid Limited
Manufacturer SRN
IN-MF-000033199
Manufacturer country
India

Covered devices

  • Pregnancy hCG Test Kit IVDR Class B
    890600528cuphcgKG