SCHWIND AMARIS - Indonesia BPOM Medical Device Registration
SCHWIND AMARIS is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21203121953. The device is manufactured by SCHWIND EYE-TECH-SOLUTIONS GMBH from Germany, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. TRIASTRI MEDITAMA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
SCHWIND EYE-TECH-SOLUTIONS GMBHCountry of Origin
Germany
Authorized Representative
PT. TRIASTRI MEDITAMAAR Address
JL. INDUSTRI NO.9-11 GUNUNG SAHARI UTARA,
Registration Date
Jun 13, 2023
Expiry Date
May 01, 2027
Product Type
Surgical Eye Equipment
Ophthalmic excimer laser system
Non Radiation Electromedics
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