REICHERT TF50 Trial Frame - Indonesia BPOM Medical Device Registration
REICHERT TF50 Trial Frame is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11201420214. The device is manufactured by LIANYUNGANG TIANNUO OPTICAL INSTRUMENT CO., LTD. from China, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. SURGIKA ALKESINDO.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
LIANYUNGANG TIANNUO OPTICAL INSTRUMENT CO., LTD.Country of Origin
China
Authorized Representative
PT. SURGIKA ALKESINDOAR Address
Jl. Letjen Suprapto No.60, Gedung Indra Sentral unit G-H, Cempaka Putih
Registration Date
Dec 06, 2024
Expiry Date
Mar 06, 2027
Product Type
Diagnostic Eye Equipment
Ophthalmic trial lens frame.
Non Electromedic Non Sterile
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