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PTCA Guidewire - India CDSCO Medical Device Registration

PTCA Guidewire is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/MD/2019/000042_4167d2d482cf70301fd4d8aec499ad2d_45f3429c8b2ca08dc8b4cf70096d0f58. This device is marketed under the brand name Explorer. The license holder is Dolphin Lifescience India LLP, and it is classified as Device Class Class D. The approving authority is Central Drug Standards Control Organization, Ahmedabad.

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.

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CDSCO Registered
Class Class D
PTCA Guidewire
UID: MFG/MD/2019/000042_4167d2d482cf70301fd4d8aec499ad2d_45f3429c8b2ca08dc8b4cf70096d0f58

Brand Name

Explorer

Device Class

Class D

Approving Authority

Central Drug Standards Control Organization, Ahmedabad

Product Information

Mariner PTCA Guidewires are steerable guidewires that are used during the Percutaneous Coronary Intervention (Explorer) to reach a lesion or vessel segment by serving as a guiding for other diagnostic or interventional devices in the coronary and peripheral vasculature.

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