Guidewire - India CDSCO Medical Device Registration

Guidewire is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2021/000082_6f79c5dae2a086e749af43b13df8e910_a89d160a5c3caf64c7b6d571ce9b4ce2. This device is marketed under the brand name Chaperon. The license holder is Faith Biotech Pvt. Ltd., and it is classified as Device Class Class D. The approving authority is CDSCO.

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CDSCO Registered

Class Class D

Guidewire

UID: IMP/MD/2021/000082_6f79c5dae2a086e749af43b13df8e910_a89d160a5c3caf64c7b6d571ce9b4ce2

Brand Name

Chaperon

License Holder

Faith Biotech Pvt. Ltd.

Device Class

Class D

Approving Authority

CDSCO

Product Information

Traxcess Guidewire is intended for general intravascular use, including the neuro and peripheral vasculature. The guidewire can be steered to facilitate the selective placement of diagnostic or therapeutic catheters. This device is not intended for use in coronary arteries.

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Guidewire

Brand: Flow Re-Direction Endoluminal Device

Class D