The “La-med” team has more than a decade of combined experience in the manufacturing, distribution and marketing of high-end single-use medical devices. Combined with the backing of strong professional and sophiscated manufacturing facilities, we are equipped to cater to the most demanding clients adhering to stringent deadlines.

Spread over a sprawling 75, 000 sq with the scope for further expansion, our flagship unit is equipped to deliver close to 150 million finished devices annually. With clean rooms meeting Class 10,000 standards designed as per the US- FDA & ISO guidelines, a controlled environment through HEPA filtration implementaon and compliance with all relevant national and global standards like strict hygiene standards of our own.

Six Sigma processes controls and TQM measures have been built into our processes rather than being externally implemented.

The manufacturing involves product design injection molding in class 100,000 controlled environment; assembly, packaging and online printing in class 10,000 cleanroom; in-house sterilization facility, Physical, chemical and biological testing in a modern in-house laboratory. In compliance with European Council Directive 93/42/ EEC of 14 June 1993 concerning medical devices, as amended by 2007/47/EEC, ISO 14971:2012 Drugs and cosmetics act 1940 & Rules 1945 of India and Medical device rule 2017 ect.

We not only comply to international authorises, but utilize this as a base to build on, by implementing it.

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