SUPORE Trial Lens - Indonesia BPOM Medical Device Registration
SUPORE Trial Lens is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11201918748. The device is manufactured by SHANGHAI SUPORE INSTRUMENTS CO., LTD. from China, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. ALFA INTERNAL OPTINDO.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
SHANGHAI SUPORE INSTRUMENTS CO., LTD.Country of Origin
China
Authorized Representative
PT. ALFA INTERNAL OPTINDOAR Address
JALAN KAREL SATSUIT TUBUN NOMOR 72 LANTAI 1 RT.001 / RW.001
Registration Date
Jun 06, 2024
Expiry Date
Dec 01, 2028
Product Type
Diagnostic Eye Equipment
Ophthalmic trial lens set.
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