.jpg)
CDSCO will be the relevant licensing authority who will approve the packages for Nebulizers manufacturing process in India. The manufacturer needs to use it for CDSCO manufacturing license and our crew will let you whole the licensing system. The producer of this merchandise should comply with the protection and efficacy foremost as consistent with the given recommendations. The individual that desires to start the nebulizer manufacturing unit needs to be privy to production and regulatory techniques. Usually, nebulizers are available in both electric or battery-run variations, and are each portable (so that you can deliver with you) or intended to take a seat down on a table and plug right into a wall.
each version of nebulizers is made of:
- a base that holds an air compressor
- a small container for liquid remedy
- a tube that connects the air compressor to the drugs box
- Above the medicine field is a mouthpiece or mask you operate to inhale the mist.
Technical Features of Nebulizer manufacturing:
- Manufactured from soft, non-toxic medical grade material.
- Made from a clear aerosol mask, perfect for long use.
- Star lumen tube to avoid fortuitous blockage.
- Made up of a kink-resistant PVC tube.
- Integrated nasal clip for stable fixation over the patient’s nose.
- Elastic strap/band is for proper mask placement.
- Tube length: 200cm.
Nebulizers Manufacturing Process:
- Injection Moulding Machine
- Sterilization plant
Raw Material Used in Nebulizer Manufacturing:
- Polyvinyl chloride (PVC)
- Elastic strap/band
- Acrylonitrile butadiene styrene (ABS)
- Polypropylene (PP)
- High density polyethylene (HDPE)
Read More - Nebulizer Manufacturing
Contact details –
Phone no - 93702 83428
Mail id – enquiry@operonstrategist.com
Read More Article -
Phone no - 93702 83428
Mail id – enquiry@operonstrategist.com
If You Want Medical Devices Services Consultation For Following.- Medical Device Consulting
- cdsco registration
- FDA 510k Clearance
- ce mark medical device
- CDSCO Manufacturing License
- CDSCO import license
- TURNKEY PROJECT CONSULTANT
- medical device manufacturing
- iso 15378 certification
- 21 cfr part 210 and 211
- ISO 13485 Medical Device Consultant
- Primary Packaging Turnkey Project Consultant
- Clean Room Design Consultant
- manufacturing site conceptualization
- Market Analysis and feasibility for Medical Devices
- manufacturing plant layout design
- medical device design and development
- DMF file submission guideline
- 21 cfr part 820
- qms certification services
- capa management
- design control requirements
- medical device process validation
- combination product
- continuous improvement program
- Medical Device Compliance & Regulatory Services
- Cdsco India authorized agent for medical device
- Medical Device Consulting
- cdsco registration
- FDA 510k Clearance
- ce mark medical device
- CDSCO Manufacturing License
- CDSCO import license
- TURNKEY PROJECT CONSULTANT
- medical device manufacturing
- iso 15378 certification
- 21 cfr part 210 and 211
- ISO 13485 Medical Device Consultant
- Primary Packaging Turnkey Project Consultant
- Clean Room Design Consultant
- manufacturing site conceptualization
- Market Analysis and feasibility for Medical Devices
- manufacturing plant layout design
- medical device design and development
- DMF file submission guideline
- 21 cfr part 820
- qms certification services
- capa management
- design control requirements
- medical device process validation
- combination product
- continuous improvement program
- Medical Device Compliance & Regulatory Services
- Cdsco India authorized agent for medical device
No comments:
Post a Comment