VISUFIT 1000 Platform - Indonesia BPOM Medical Device Registration
VISUFIT 1000 Platform is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11201220093. The device is manufactured by CARL ZEISS JENA GMBH from Germany, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PERFECT SINGLE OPTICS.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
CARL ZEISS JENA GMBHCountry of Origin
Germany
Authorized Representative
PERFECT SINGLE OPTICSAR Address
Jl. Pintu Air Raya No. 36 KL. Pasar baru
Registration Date
Jun 21, 2022
Expiry Date
Sep 30, 2025
Product Type
Diagnostic Eye Equipment
Ophthalmic refractometer.
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