Biongraft Putty - Indonesia BPOM Medical Device Registration
Biongraft Putty is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21302420234. The device is manufactured by BONEGRAFT BIOLOGICAL MATERIALS SAN. A.Ş. (BONEGRAFT A.Ş.) from Turkey, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is SPEAKING OF MEDICS..
This page provides comprehensive regulatory information including complete registration details, manufacturer information, authorized representative details, product classification, and related products. Pure Global AI offers free access to 67,600+ Indonesia medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.
Risk Classification
Product Class
Kelas : 2
Country of Origin
Turkey
Authorized Representative
SPEAKING OF MEDICS.AR Address
RUKO THE HIVE CENDANA PARC, JALAN CENDANA PARC RAYA 1 NO. 65 LIPPO VILLAGE
Registration Date
Jul 08, 2024
Expiry Date
Feb 19, 2027
Product Type
Prosthetic Orthopedic Equipment
Resorbable calcium salt bone void filler device.
Non Electromedic Sterile

