Algaflex Line - India CDSCO Medical Device Registration

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.

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CDSCO Registered

Class Class B

Algaflex Line

UID: IMP/MD/2020/000101_1c958b0ae092c06ecfbe833b146fe863_a610c6efda50cac3fa3b08e1f8102681

Brand Name

MANIFOLD

License Holder

VYGON INDIA PRIVATE LIMITED

Device Class

Class B

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