GMD is manufacturing a range of sterilized absorbable and non-absorbable surgical sutures, as per United States pharmacopoeia (USP) & European pharmacopoeia (EP).
In a clean room class 10,000, we operate with a quality assurance system, taking care for every single suture, and make sure that every batch had been tested and passed all the Examinations.
A highly educated and qualified team take the responsibility of manufacturing sutures from raw materials to the finished product stage enabling us to guarantee Product Reliability and Customer Satisfaction.
High technology of testing facility to conduct all related Chemical, Instrumental and Microbiological Tests to guarantee final product quality.
Our Products meet the requirements of the European Medical Device Directive 93/42/EEC and, European pharmacopoeia (Ph Eur.) and United States pharmacopoeia (U.S.P.)
Our Products meet the requirements of the European Medical Device Directive 93/42/EEC and, European pharmacopoeia (Ph Eur.) and United States pharmacopoeia (U.S.P.)
