SYNOLIS VA 80/160 - Indonesia BPOM Medical Device Registration
SYNOLIS VA 80/160 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 31302320986. The device is manufactured by SKIN TECH PHARMA GROUP, S.L from Spain, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is PT. I-TECH LAFACOS.
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Risk Classification
Product Class
Kelas : 3
Manufacturer
SKIN TECH PHARMA GROUP, S.LCountry of Origin
Spain
Authorized Representative
PT. I-TECH LAFACOSAR Address
Gedung indra centra Blok M-N, Jl. Jendral suprapto No. 60, Kel Cempaka Putih barat , Kec. Cempaka Putih
Registration Date
Nov 14, 2023
Expiry Date
Aug 15, 2026
Product Type
Prosthetic Orthopedic Equipment
Intra articular fluid
Non Electromedic Sterile
DISCOVERY Pico Derm
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