Meridian MR Q SLT - Indonesia BPOM Medical Device Registration
Meridian MR Q SLT is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21203420198. The device is manufactured by MERIDIAN MEDICAL D.O.O. from Slovenia, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. PERFECT SINGLE OPTICS.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
MERIDIAN MEDICAL D.O.O.Country of Origin
Slovenia
Authorized Representative
PT. PERFECT SINGLE OPTICSAR Address
Jalan Pintu Air Raya No. 36 K-L
Registration Date
Sep 23, 2024
Expiry Date
May 20, 2029
Product Type
Surgical Eye Equipment
Nd:YAG laser for posterior capsulotomy and peripheral iridotomy.
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