IRES NX001 - Indonesia BPOM Medical Device Registration
IRES NX001 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21203220170. The device is manufactured by IVIS TECHNOLOGIES S.R.L from Italy, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. HARLISA TRUE GRACE.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
IVIS TECHNOLOGIES S.R.LCountry of Origin
Italy
Authorized Representative
PT. HARLISA TRUE GRACEAR Address
Perum Sedati Permai Jl. Sriti HH-15
Registration Date
Nov 23, 2022
Expiry Date
Jul 22, 2027
Product Type
Surgical Eye Equipment
Ophthalmic excimer laser system
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