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Knee Arthroplasty Kit - India CDSCO Medical Device Registration

Knee Arthroplasty Kit is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/MD/2019/000230_ab84c2f337d87107a249d40227ae43ba_d0f9ec7275fecfaa1cf7c84fbc69567e. This device is marketed under the brand name Bylatoral Femoral Bypass Surgery Kit. The license holder is Lotus Surgical Pvt Ltd, and it is classified as Device Class Class D. The approving authority is CDSCO -North Zone, Ghaziabad.

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
Knee Arthroplasty Kit
UID: MFG/MD/2019/000230_ab84c2f337d87107a249d40227ae43ba_d0f9ec7275fecfaa1cf7c84fbc69567e

Brand Name

Bylatoral Femoral Bypass Surgery Kit

Device Class

Class D

Approving Authority

CDSCO -North Zone, Ghaziabad

Product Information

Intended used for surgical dressing and control blood loss during Knee arthroplasty. Knee arthroplasty, is a surgical procedure in which parts of the knee joint or the weight-bearing surfaces are replaced with artificial parts s a surgical procedure to relieve pain and disability

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