REVANESSE ULTRA+ - Indonesia BPOM Medical Device Registration
REVANESSE ULTRA+ is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 31602220093. The device is manufactured by PROLLENIUM MEDICAL TECHNOLOGIES INC. from Canada, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is PT. MENJANGAN SAKTI.
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Risk Classification
Product Class
Kelas : 3
Manufacturer
PROLLENIUM MEDICAL TECHNOLOGIES INC.Country of Origin
Canada
Authorized Representative
PT. MENJANGAN SAKTIAR Address
Jl. HR. Rasuna Said Kav. B-34 Kuningan
Registration Date
Sep 28, 2022
Expiry Date
Jul 07, 2024
Product Type
Prosthetic Surgical Equipment
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