CIGARS Dermis Allograft - Indonesia BPOM Medical Device Registration
CIGARS Dermis Allograft is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20602320840. The device is manufactured by RTI SURGICAL, INC from United States, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. TAWADA HEALTHCARE.
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PUROS Dermis Allograft
Risk Classification
Product Class
Kelas : 2
Manufacturer
RTI SURGICAL, INCCountry of Origin
United States
Authorized Representative
PT. TAWADA HEALTHCAREAR Address
Rukan Permata Senayan Blok A18-19 Lantai 1-2 Jl. Tentara Pelajar No. 5
Registration Date
Nov 30, 2023
Expiry Date
Jun 19, 2028
Product Type
Prosthetic Dental Equipment
Bone grafting material.
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