Algaflex Line
- UID
- IMP/MD/2020/000101_1c958b0ae092c06ecfbe833b146fe863_a610c6efda50cac3fa3b08e1f8102681
- Device class
- Class B
- Brand name
- MANIFOLD
- License holder
- VYGON INDIA PRIVATE LIMITED
- Approving authority
- CDSCO
- Product information
- The ALGAFLEX lines are designed to connect two devices for the purpose of conveying a liquid such as contrast liquid or serum under a given pressure. Simply connect the female end to the male end of a device and the male end to the female end of another device. Algaflex lines are intended to be connected to an angiography syringe on one side and to a catheter on the other side to allow the injection of contrast media to the patient. These devices are used in interventional radiology during angiography and angioplasty procedures for the high-pressure line
Algaflex Line is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2020/000101_1c958b0ae092c06ecfbe833b146fe863_a610c6efda50cac3fa3b08e1f8102681. This device is marketed under the brand name MANIFOLD. The license holder is VYGON INDIA PRIVATE LIMITED, and it is classified as Device Class Class B. The approving authority is CDSCO.
This page provides comprehensive regulatory information including complete registration details, license holder information, device classification, and related products. Pure Global AI offers free access to 71,807+ India medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.