DURAGEN Plus Dural Regeneration Matrix - Indonesia BPOM Medical Device Registration
DURAGEN Plus Dural Regeneration Matrix is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21003615406. The device is manufactured by INTEGRA LIFESCIENCES CORPORATION from United States, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. TRIDAYA MEDICAL SYNERGY.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
INTEGRA LIFESCIENCES CORPORATIONCountry of Origin
United States
Authorized Representative
PT. TRIDAYA MEDICAL SYNERGYAR Address
Jl. BSD Grand Boulevard, BSD Green Office Park, BSD City, Wing B, 3rd floor, Zone 7C
Registration Date
Aug 02, 2023
Expiry Date
Mar 31, 2025
Product Type
Therapeutic Neurology Equipment
Dura substitute.
Non Electromedic Sterile
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