Certified quality you can independently verify.
Third-party ISO 6710:2017 certification plus compliance with WHO-GMP, CE and SSI standards — the assurance distributors and laboratories need.
Independently certified
ISO 6710:2017
Single-use containers for human venous blood specimen collection
Designing, developing, manufacturing & export of all kinds of plastic medical devices — vacuum and non-vacuum blood collection tubes, plastic cassettes for IVD rapid diagnostic test kits, buffer reagent bottles and disposable laboratoryware items.
- Certificate number
- UQ-2024031832
- Standard
- ISO 6710:2017
- Certifying body
- UK Certifications
- Validity
- Valid to 17 March 2027
Certificate scope covers the design, development, manufacture and export of vacuum and non-vacuum blood collection tubes and related plastic medical devices.
Standards we manufacture to
CE
Products manufactured in conformity with the applicable European directives for in vitro diagnostic devices.
WHO · GMP
Manufacturing operations run to WHO Good Manufacturing Practice standards for medical device production.
SSI
Adherence to SSI regulatory standards as part of the company's quality management framework.
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