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/2021/000005_6f79c5dae2a086e749af43b13df8e910_25de71c1f7ed6e0ef28f2f0e71544d4e. This device is marketed under the brand name PrymaX Angi. The license holder is Prymax Healthcare LLP,, and it is classified as Device Class Class D. The approving authority is Sub Zonal Baddi.

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CDSCO Registered

Class Class D

Guidewire

UID: MFG/MD/2021/000005_6f79c5dae2a086e749af43b13df8e910_25de71c1f7ed6e0ef28f2f0e71544d4e

Brand Name

PrymaX Angi

License Holder

Prymax Healthcare LLP,

Device Class

Class D

Approving Authority

Sub Zonal Baddi

Product Information

Guidewire facilitates placement of a catheter during diagnostic or interventional peripheral intravascular procedures including but not limited to renal intervention. The wire can be torqued to facilitate navigation through the vasculature.