Medical Disposal
Single-use and disposable products for everyday clinical use.
0
International &
Regional Markets
I-TEC runs an R&D team and a production facility in Singapore. Every product is designed, registered and released under the I-TEC name, which means the regulatory responsibility sits with us rather than a client.
Where a product calls for specialist capability, we work with selected manufacturers worldwide. The specification, the certification and the pricing stay with us. Our products reach hospitals, pharmacies, government agencies and retail partners in Singapore and internationally.
More About I-TEC
Every product carries our name because we developed it, tested it and stand behind it.
How We Work
Each product begins with our R&D team in Singapore and is manufactured at our facility. Where a product calls for specialist capability, we bring in selected manufacturing partners under our specification and our quality control. Behind every product is a technical file, a test history and a registration in I-TEC’s name. That documentation is what allows a product into 25 markets, and it belongs to us.
The I-TEC product cycle
What stays with us
Research And Validation
We work with reputable research centres and regional partners to conduct clinical trials and product studies during development. Safety and usability are established before a product is distributed into any market.
I-TEC is registered with Singapore's Health Sciences Authority, and our products are tested by independent laboratories. The resulting test reports and registration records are kept on file and available for buyers to review.
It isn't a shipping label. It's a declaration that the product was actually manufactured here, at our own facility, under Singapore's regulatory framework, not imported and relabelled.
When you see this mark on I-TEC packaging, the manufacturing, quality control and certification behind that product all happened on our own production floor in Singapore.
Browse the I-TEC range, made for hospitals, pharmacies, retail partners and institutional buyers.
Not sure which product fits your requirements? Our team can help you review the available options.
Single-use and disposable products for everyday clinical use.
Equipment for hospital wards and clinical facilities.
Medical-grade masks for healthcare and facility use.
Diagnostic and clinical devices for healthcare settings.
Regional Network
Our R&D, our registrations and our quality control all run from Singapore. The products reach hospitals, pharmacies and retail partners across Asia, Europe and North America.
Our Network
The four things buyers check, and where we stand on each.
Our own R&D team develops each product. Design and development sit inside our ISO 13485 certified scope.
Coordinate supply across 25 international and regional markets, from one point of contact.
Verified certifications and compliance records to ensure our products meet international standards and safety requirements.
Trusted and distributed at hospitals, pharmacies and reputable distributors around the world.
Documentation and Compliance
I-TEC holds ISO 13485 and CE certification covering design, development and production, backed by independent lab testing and verified company registration, available for hospitals, distributors and procurement teams to review before progressing with an order.
For certification documentation specific to your order, contact our team directly.
1 / 17
Product Categories
How to read ASTM F2100-19 and EN 14683:2019 mask ratings, and which mask type fits which use case.
Read ArticleRegional Supply
Get In Touch
Tell us which I-TEC products you need, the destination market and estimated quantity, and our team will follow up with pricing and documentation.