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Bone screw - India CDSCO Medical Device Registration

Bone screw is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/MD/2019/000085_38dd9160e1dff87270cbde32ec4a5a30_64c4b20f3ee2c74310a826a1e8e4a980. This device is marketed under the brand name Seinser/Actose/Rootsure/Joibis. The license holder is Pehchan Pharmaceuticals And Surgicals LLP, and it is classified as Device Class Class C. 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 C
Bone screw
UID: MFG/MD/2019/000085_38dd9160e1dff87270cbde32ec4a5a30_64c4b20f3ee2c74310a826a1e8e4a980

Brand Name

Seinser/Actose/Rootsure/Joibis

Device Class

Class C

Approving Authority

Central Drug Standards Control Organization, Ahmedabad

Product Information

The Bone Screw is intended for internal fixation of fractures and reconstruction of bones including the Scapula, Olecranon, Humerus, Radius, Ulna, Pelvis, Distal, Tibia, Fibula, Hand and Foot in adults and for long bones in adolescents in whom the growth plates are fused. It can be used with or without the plates

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