Guidewire - India CDSCO Medical Device Registration

Guidewire is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/MD/2021/000194_6f79c5dae2a086e749af43b13df8e910_51935dc7f508d2d4dd6a8c24df654978. This device is marketed under the brand name AngiX. The license holder is BL Lifesciences Pvt. Ltd., and it is classified as Device Class Class D. The approving authority is CDSCO -North Zone, Ghaziabad.

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CDSCO Registered

Class Class D

Guidewire

UID: MFG/MD/2021/000194_6f79c5dae2a086e749af43b13df8e910_51935dc7f508d2d4dd6a8c24df654978

Brand Name

AngiX

License Holder

BL Lifesciences Pvt. Ltd.

Device Class

Class D

Approving Authority

CDSCO -North Zone, Ghaziabad

Product Information

The Guide wire is used to access the vein or artery while inserting the cannula or sheath in to the vessel. This is used for proper positioning of the device.

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Guidewire

Brand: Non-sterile

Class C