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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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Daysoft Limited

Certificate GB25/00000187

Rev. 1Issued
Valid until
Oct 14, 2030

Certificate GB25/00000187 is a valid Quality assurance issued to Daysoft Limited and registered in EUDAMED. Valid until October 14, 2030. View the full certificate record on MD Atlas.

Overview

Certificate number
GB25/00000187
Certificate type
Quality assurance
Certificate status
Issued
Applicable legislation
MDR [Regulation (EU) 2017/745 on medical devices]
Version
1
Certificate ID
1639GB25/000001871

Validity

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

Notified body

Notified body
SGS Belgium NV
Notified body SRN
1639
Notified body country
Belgium

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 IIa2

2 scopes

  • MDN1206, MDS1005
    Class IIa
  • Sterile cast moulded one-day disposable hydrogel contact lenses
    Class IIa

Documents

LanguagesEN

Manufacturer

Manufacturer
Daysoft Limited
Manufacturer SRN
GB-MF-000006737
Manufacturer country
United Kingdom