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 31003420115. The device is manufactured by INTEGRA LIFESCIENCES CORPORATION from United States, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is PT. TRIDAYA MEDICAL SYNERGY.
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 : 3
Manufacturer
INTEGRA LIFESCIENCES CORPORATIONCountry of Origin
United States
Authorized Representative
PT. TRIDAYA MEDICAL SYNERGYAR Address
Foresta Business Loft 6 Unit 2, Jl. BSD Boulevard Utara, Kelurahan Lengkong Kulon, Kecamatan Pagedangan, Kabupaten Tangerang, Banten 15331, Indonesia
Registration Date
Nov 03, 2024
Expiry Date
Mar 31, 2027
Product Type
Therapeutic Neurology Equipment
Dura substitute
Non Electromedic Sterile
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