Production Facilities

As a manufacturer of medical disposable, Angiplast maintains controlled environment for the assembly of medical components and molding of select components. The environmental controls in place are intended solely to reduce the contaminants.

Angiplast’s manufacturing capability includes:

As maintaining the quality is assumed to be the key to success and incorporated as a strategic plan. ANGIPLAST has in-house ETO capabilities ensuring quick turnaround times for our clients.

ISO 13485 certification CE certification FDA registration GMP compliance products using state of the art technology in ultra modern facilities covering over 50000 square feet of manufacturing floor space with Clean room of Class 10000.

Understanding the importance of clean room in the company, we possess complaint and adept workforce of over 300 employees. The team is supported by talented engineering and R&D team. To ensure accuracy and that all the guidelines of clean room are maintained, the team also consists of veteran management professional with strong commitment to maintain quality, excellence and smooth flow of services.

The Quality Control Laboratory has been certified to perform biological, chemical, microbiological, physical, sterility and toxicity tests. The Laboratory is equipped with state-of-the-art technology and staffed with qualified trained personal.

Quality Control System at Angiplast encompasses a systematic, fully documented, comprehensive and exhaustive series of bacteriological, chemical, physical and visual tests; and inspections at each pertinent stage in the production cycle. This involves constant surveillance of raw-materials, intensive in process control of all manufactured parts, sub-assemblies and final inspection and testing of the finished products.