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Enter your Category 1 Description Here
Invitech and BioMedica Diagnostics are pleased to announce that ACTICLOT® C (REF ACC-45) is now CE marked. Notification has been made to the Belgian Competent Authority that the product fully complies with the In Vitro Diagnostic Directive (IVDD) 98/79 of the European Parliament and of the Council.
ACTICLOT C is intended for the measurement of Protein C activity in human plasma via an endpoint clotting assay.
Due to the adverse weather there will be no staff in the Invitech office on Monday 25th January 2021.
Unfortunately no orders will ship today.
We apologise for any inconvenience.
LDN has made revisions to the Plasma Metanephrine/Normetanephrine ELISAs.
These revisions have become necessary due to the IVDR regulations (EU) 2017/746.
The following kits are affected by these changes:
We have been informed by LDN that there are assay revisions of the following kits
|
Metanephrine Plasma ELISA Fast Track |
BA E-8100 |
|
Metanephrine Plasma ELISA Fast Track (RUO) |
BA E-8100R |
|
Normetanephrine Plasma ELISA Fast Track |
BA E-8200 |
|
Normetanephrine Plasma ELISA Fast Track (RUO) |
BA E-8200R |
|
2-MET Plasma ELISA Fast Track |
BA E-8300 |
|
2-MET Plasma ELISA Fast Track (RUO) |
BA E-8300R |
which will affect the assays to some extent.
The outcome of the EU membership referendum on 23rd June 2016 meant that the UK will leave the European Union, or ‘Brexit’ as it has become known. Inevitably there is still uncertainty as the Brexit negotiations take place, whatever the outcome may be, our customers can be assured of our best endeavours to mitigate risks to their supply chain.
The UK has left the European Union and transitional arrangements will cease on 31st December 2020. There is still uncertainty as the Brexit negotiations continue but, whatever the outcome may be, our customers can be assured of our best endeavours to mitigate risks to their supply chain.