
DIVINE INDIA
MEDICAL MANUFACTURING
Manufacturing Facility
World-class infrastructure meeting international standards for medical device manufacturing.
OUR FACILITY
Modern Manufacturing
Infrastructure
Divine India operates a purpose-built manufacturing facility designed specifically for medical device production. Our facility incorporates the latest technology and best practices to ensure consistent quality and compliance with international standards.
​
Spanning over 10,000 square feet, our facility houses Class 10,000 clean rooms, dedicated production lines, quality control laboratories, and in-house sterilization capabilities.​
ISO-compliant manufacturing processes
Dedicated clean room areas
Advanced machinery and equipment
Trained and certified personnel
Regular facility audits and maintenance
State-of-the-Art Facility
10,000+ sq ft manufacturing space with modern equipment
HEPA Filtration
Advanced air filtration ensuring particle-free environment
Climate Control
Controlled temperature (18-24°C) and humidity (35-65% RH)
EO Sterilization
In-house Ethylene Oxide sterilization chamber
Class 10,000 Clean Room
Our Class 10,000 (ISO 7) clean room provides a controlled environment with less than 10,000 particles (0.5 micron or larger) per cubic foot of air. This ensures sterile product manufacturing with minimal contamination risk.
Clean Room Features:
Air Changes
Temperature
Humidity
Pressure
20-30 per hour
35-65% RH
18-24°C
Positive +15 Pa
HEPA filtered air supply
Continuous environmental monitoring
Personnel airlocks and gowning areas
Material transfer hatches
Regular validation and certification
In-House EO Sterilization
Our facility features an in-house Ethylene Oxide (EO) sterilization chamber, allowing us to provide complete sterilization services for all our products. This ensures faster turnaround times and complete quality control.
Sterilization Process:
1. Pre-conditioning and humidification
2. EO gas exposure at controlled parameters
3. Evacuation and air washes
4. Aeration period for residual gas removal
Validated sterilization cycles
Biological indicator testing
Complete cycle documentation
Regular equipment calibration
Residual EO testing
Manufacturing Process Flow
Our systematic approach ensures consistent quality at every stage of production
Raw Material Inspection
Rigorous quality checks of all incoming materials
01
Clean Room Production
Manufacturing in controlled Class 10,000 environment
02
In-Process Quality Control
Continuous monitoring and testing during production
03
EO Sterilization
Validated sterilization process for sterile products
04
Final Quality Testing
Comprehensive testing before release
05
Packaging and Dispatch
Custom packaging and timely delivery