Resorbable Bilayer Membrane - India CDSCO Medical Device Registration

Resorbable Bilayer Membrane is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2019/000069_d4b0522eba8f7259c7da21e352ea9a33_24f29ba0b9a4b0ee0d5135e39bb17cb5. This device is marketed under the brand name Geistlich Bio-Gide. The license holder is M/s Geistlich Pharma India Pvt. Ltd., and it is classified as Device Class Class D. The approving authority is CDSCO.

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.

Free Database

CDSCO Registered

Class Class D

Resorbable Bilayer Membrane

UID: IMP/MD/2019/000069_d4b0522eba8f7259c7da21e352ea9a33_24f29ba0b9a4b0ee0d5135e39bb17cb5

Brand Name

Geistlich Bio-Gide

License Holder

M/s Geistlich Pharma India Pvt. Ltd.

Device Class

Class D

Approving Authority

CDSCO

Product Information

Geistlich Bio-Gide Perio, Geistlich Bio-Gide Compressed are intended to be used as barrier membranes in the regeneration of bone defects. Geistlich Bio-Gide Perio, Geistlich Bio-Gide Compressed are used after bone grafting procedures and to enhance soft tissue formation: a) GBR (Geistlich Bio-Gide) procedures b) Immediate or delayed augmentation around implants placed in extraction sockets c) Reconstruction of the alveolar ridge d) Filling of bone defects in the maxillofacial area e) Cleft closure surgeries Geistlich Bio-Gide Perio is especially indicated for periodontal bone defects. Geistlich Bio-Gide Shape is intended to be used as a barrier membrane in the regeneration of alveolar bone defects. Geistlich Bio-Gide Shape is used for alveolar bone defects in extraction sockets