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According to CDSCO guidelines, Cardiopulmonary bypass cardiotomy suction line blood falls under Risk Class B under Cardiovascular category of Medical Devices. Intended use - A cardiopulmonary bypass cardiotomy suction line blood filter is a device used as part of a gas exchange (oxygenator) system to filter nonbiologic particles and emboli (a blood clot or a piece of foreign material flowing in the bloodstream which will obstruct circulation by blocking a vessel) out of the blood. This device is intended for use in the cardiotomy suction line.. This article will give you complete information about manufacturing Cardiopulmonary bypass cardiotomy suction line blood

According to CDSCO guidelines, Chemical cold pack snakebite kit. falls under Risk Class D under General Hospital/Orthopaedic category of Medical Devices. Intended use - Intended for first-aid treatment of snakebites. This article will give you complete information about manufacturing Chemical cold pack snakebite kit.

According to CDSCO guidelines, Cranial electrotherapy stimulator. falls under Risk Class D under Neurological category of Medical Devices. Intended use - A cranial electrotherapy stimulator is a device that applies electrical current to a patient's head to treat insomnia, depression, or anxiety. This article will give you complete information about manufacturing Cranial electrotherapy stimulator.

According to CDSCO guidelines, Pliable-polymer dental regeneration membrane, bio absorbable, ligated falls under Risk Class C under Dental category of Medical Devices. Intended use - A sterile bio absorbable material intended to be used to aid in the regeneration of tooth support, lost due to periodontal disease or trauma, by acting as a barrier to prevent the down-growth of soft tissue (connective tissue and epithelial cells) into the underlying bone during the healing period.. This article will give you complete information about manufacturing Pliable-polymer dental regeneration membrane, bio absorbable, ligated

According to CDSCO guidelines, Probiotic oropharyngeal mucosa dressing falls under Risk Class C under Gastroenterology category of Medical Devices. Intended use - A non-sterile substance intended to be applied to the mucosa of the mouth and/or pharynx to facilitate saprophytic microflora colonization within the oral cavity/pharynx, typically following antibiotic therapy, bacterial infection, or injury. It includes probiotic bacteria (e.g., Streptococcus salivarius, Streptococcus oralis) and compounds that create a barrier to facilitate growth of the probiotic bacteria.. This article will give you complete information about manufacturing Probiotic oropharyngeal mucosa dressing