V30 - Indonesia BPOM Medical Device Registration
V30 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603716345. The device is manufactured by VIORA LTD. from Israel, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is SURGIKA ALKESINDO.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
VIORA LTD.Country of Origin
Israel
Authorized Representative
SURGIKA ALKESINDOAR Address
Jl. Letjen Suprapto No.60, Gedung Indra Sentral unit G-H, Cempaka Putih
Registration Date
Jul 12, 2022
Expiry Date
Jun 22, 2025
Product Type
Surgical Equipment
Laser surgical instrument for use in general and plastic surgery and in dermatology.
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