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Post Dilatation Catheter - India CDSCO Medical Device Registration

Post Dilatation Catheter is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/MD/2022/000294_b36a9a53901cff7a32a0854da5c52f46_53121afe3a95a488ab4fe64e65096d2a. This device is marketed under the brand name Pearsilk, Silkfil.. The license holder is Multimedics LLP, and it is classified as Device Class Class C. The approving authority is Sub Zonal Baddi.

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 C
Post Dilatation Catheter
UID: MFG/MD/2022/000294_b36a9a53901cff7a32a0854da5c52f46_53121afe3a95a488ab4fe64e65096d2a

Brand Name

Pearsilk, Silkfil.

License Holder

Multimedics LLP

Device Class

Class C

Approving Authority

Sub Zonal Baddi

Product Information

1.1. Balloon dilatation of the stenotic portion of a coronary artery or bypass graft stenosis, for the purpose of improving myocardial perfusion. 1.2. Balloon dilatation of a coronary artery occlusion, for the purpose of restoring coronary flow in patients with ST-segment elevation myocardial infarction. 1.3. Balloon dilatation of a stent after implantation.

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