Branded lateral flow tests, documentation and sales representation for professional in vitro diagnostic markets outside the United States.
First Diagnostic™ Corporation provides rapid test distribution services for distributors, public health programs, hospitals, laboratories and clinics outside the United States. The company, founded in 2004, brands and distributes lateral flow rapid tests made by established IVD manufacturers.
It also offers sales representation to diagnostic manufacturers. Commercial terms are not published here; they are set out in writing for each inquiry.
ATFirst™ general rapid tests and inSTIcheck™ sexually transmitted infection tests, supplied to qualified distributors for professional in vitro diagnostic use.
Applicants describe their company, market and regulatory capability. Each application is reviewed before supply is discussed.
Product inserts are available to download. Regulatory documents are provided on request.
The Country Station sets out rapid test supply by region, so a buyer can start from the destination market.
Private-label requests are discussed case by case; labeling and regulatory responsibilities are defined in writing with the manufacturer.
Diagnostic manufacturers can ask First Diagnostic to represent their products to professional buyers.
Instructions for use can be downloaded from the product inserts page, and other inserts are sent on request. Regulatory documents are also provided on request; see quality and regulatory information for details.
Regulatory status and availability vary by country. The Country Station for regional rapid test supply is the starting point for a specific market.
A manufacturer’s representative promotes and sells a manufacturer’s products to buyers on the manufacturer’s behalf. Our guide to what a manufacturer’s representative does explains the model, and the page on sales representation for diagnostic manufacturers describes how First Diagnostic approaches it. Scope and responsibilities are agreed in writing for each product line.
No prices, delivery times, territories or exclusivity are offered on this website. They are discussed individually and confirmed only in writing.
Qualified distributors, public health programs, hospitals, laboratories and clinics outside the United States. All tests are for professional in vitro diagnostic use.
Product inserts, by download or on request, and regulatory documentation on request. Only some products carry the CE mark on their insert; see quality and regulatory information.
Nothing of that kind is published. Commercial terms are discussed with each qualified applicant and confirmed in writing.
Send your company details, the products or service you need and the destination country.
Regulatory status: Products shown on this website are for professional in vitro diagnostic use. They are not cleared, approved or authorized by the U.S. Food and Drug Administration and are not offered for sale in the United States. Product availability and regulatory status vary by country; contact us for the status in your market.