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Sterile Synthetic Hydroxyapatite Bone Graft - India CDSCO Medical Device Registration

Sterile Synthetic Hydroxyapatite Bone Graft is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/MD/2020/000084_f9928422042f0eddac518805fd297ab0_2c18758003299913895b6be172707a8c. This device is marketed under the brand name Sybograf. The license holder is Eucare Pharmaceuticals Private Limited., and it is classified as Device Class Class C. The approving authority is Central Drug Standard Control Organisation, South Zone.

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
Sterile Synthetic Hydroxyapatite Bone Graft
UID: MFG/MD/2020/000084_f9928422042f0eddac518805fd297ab0_2c18758003299913895b6be172707a8c

Brand Name

Sybograf

Device Class

Class C

Approving Authority

Central Drug Standard Control Organisation, South Zone

Product Information

Sterile Synthetic Hydroxyapatite Bone Graft is indicated as a hydroxyapatite graft material for Bone Regeneration procedures in Dental surgeries

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