HEINE Beta 200 Streak Retinoscope - Indonesia BPOM Medical Device Registration
HEINE Beta 200 Streak Retinoscope is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21201124393. The device is manufactured by HEINE OPTOTECHNIK GMBH & CO. KG from Germany, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. SURGIKA ALKESINDO.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
HEINE OPTOTECHNIK GMBH & CO. KGCountry of Origin
Germany
Authorized Representative
PT. SURGIKA ALKESINDOAR Address
Jl. Letjen Suprapto No.60, Gedung Indra Sentral unit G-H, Cempaka Putih
Registration Date
Apr 27, 2022
Expiry Date
Feb 28, 2025
Product Type
Diagnostic Eye Equipment
Retinoscope.
Non Radiation Electromedics
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