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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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Reckitt Benckiser Healthcare (UK) Limited

Certificate GB24/00000192

Rev. 1Issued
Valid until
Sep 10, 2029

Certificate GB24/00000192 is a valid Quality assurance issued to Reckitt Benckiser Healthcare (UK) Limited and registered in EUDAMED. Valid until September 10, 2029. View the full certificate record on MD Atlas.

Overview

Certificate number
GB24/00000192
Certificate type
Quality assurance
Certificate status
Issued
Applicable legislation
MDR [Regulation (EU) 2017/745 on medical devices]
Version
1
Certificate ID
1639GB24/000001921

Validity

Issued
Sep 10, 2024
Valid from
Sep 10, 2024
Valid until
Sep 10, 2029

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
No
Human tissues
No
Animal tissues
No
In vitro diagnostics
No
Initial registration
Yes
New device
No
Discard allowed
No
SSCP enabled
No
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 I2

2 scopes

  • MDN1202, MDS1010
    Class I
  • Graduated dosing cup to measure and administer an accurate dose of oral liquid medicine
    Class I

Documents

LanguagesEN

Manufacturer

Manufacturer
Reckitt Benckiser Healthcare (UK) Limited
Manufacturer SRN
GB-MF-000035615
Manufacturer country
United Kingdom