PLUSOPTIX 12 - Indonesia BPOM Medical Device Registration
PLUSOPTIX 12 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11201320313. The device is manufactured by PLUSOPTIX GMBH from Germany, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is TRIASTRI MEDITAMA.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
PLUSOPTIX GMBHCountry of Origin
Germany
Authorized Representative
TRIASTRI MEDITAMAAR Address
GRIYA KEMAYORAN BLOK R-41 JL. INDUSTRI RAYA NO. 9-11
Registration Date
Apr 27, 2023
Expiry Date
Dec 31, 2028
Product Type
Diagnostic Eye Equipment
Ophthalmic refractometer.
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