Rodenstock Perfalit 1.56 PRO 410 - Indonesia BPOM Medical Device Registration
Rodenstock Perfalit 1.56 PRO 410 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11204320933. The device is manufactured by SHANGHAI CONANT OPTICS CO.,LTD from China, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. SOURCE OF KENCANA BLESSINGS.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
SHANGHAI CONANT OPTICS CO.,LTDCountry of Origin
China
Authorized Representative
PT. SOURCE OF KENCANA BLESSINGSAR Address
JL. KS. TUBUN RAYA NO. 64,
Registration Date
Aug 21, 2023
Expiry Date
Jul 01, 2027
Product Type
Therapeutic Eye Equipment
Prescription show lens.
Non Electromedic Non Sterile
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