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Epidural Needle - India CDSCO Medical Device Registration

Epidural Needle is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/MD/2021/000033_c987a720499687375060841f69e859a9_c058d6da659011cd0a39eb4f1d167799. This device is marketed under the brand name VIGGO-MANIFOLD-2WAY & VIGGO-MANIFOLD-3WAY. The license holder is Viggo Medical Devices India Private Limited, and it is classified as Device Class Class B. The approving authority is Haryana.

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 B
Epidural Needle
UID: MFG/MD/2021/000033_c987a720499687375060841f69e859a9_c058d6da659011cd0a39eb4f1d167799

Brand Name

VIGGO-MANIFOLD-2WAY & VIGGO-MANIFOLD-3WAY

Device Class

Class B

Approving Authority

Haryana

Product Information

Intended for transient delivery of anesthetics to provide regional anesthesia or facilitate placement of an epidural catheter

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