OCULIGHT TX 532 SYSTEM - Indonesia BPOM Medical Device Registration
OCULIGHT TX 532 SYSTEM is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603222226. The device is manufactured by IRIDEX CORP. from United States, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. TOPSINDO MEGAH UTAMA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
IRIDEX CORP.Country of Origin
United States
Authorized Representative
PT. TOPSINDO MEGAH UTAMAAR Address
Jl. P. Jayakarta No. 55 Gedung Baja Tower C Lt. 3 Unit C 03-01
Registration Date
Sep 14, 2023
Expiry Date
Nov 07, 2026
Product Type
Surgical Equipment
Laser surgical instrument for use in general and plastic surgery and in dermatology.
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