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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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Cantor Barnard Limited

Certificate GB23/00000065

Rev. 7Cancelled
Valid until
Feb 10, 2028

Certificate GB23/00000065, a Quality management system issued to Cantor Barnard Limited, has been withdrawn. View the full certificate record on MD Atlas.

Overview

Certificate number
GB23/00000065
Certificate type
Quality management system
Certificate status
Cancelled
Applicable legislation
MDR [Regulation (EU) 2017/745 on medical devices]
Version
6
Certificate ID
1639GB23/000000657

Validity

Issued
Jan 10, 2025
Valid from
Jan 10, 2025
Valid until
Feb 10, 2028

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
No
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

Status changes

  • Cancelled

Supersedes

  • GB23/00000065Quality management systemAmendedJan 10, 2025 → Feb 10, 2028

Scope coverage

Class IIa3

3 scopes

  • RGP Lenses
    Class IIa
  • MDN1206
    Class IIa
  • Soft Sterile Contact Lense
    Class IIa

Documents

LanguagesEN

Manufacturer

Manufacturer
Cantor Barnard Limited
Manufacturer SRN
GB-MF-000009886
Manufacturer country
United Kingdom