MERIDIAN MRQ Medical Therapeutical Laser System - Indonesia BPOM Medical Device Registration
MERIDIAN MRQ Medical Therapeutical Laser System is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21203320321. 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. KATAMATA OPTOMEDIK.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
MERIDIAN MEDICAL D.O.O.Country of Origin
Slovenia
Authorized Representative
PT. KATAMATA OPTOMEDIKAR Address
Komplek Ketapang Indah Blok B2 No.31 Jl. KH. Zainul Arifin Kel.Krukut, Kec.Taman Sari Jakarta Barat
Registration Date
Jul 06, 2023
Expiry Date
May 12, 2027
Product Type
Surgical Eye Equipment
Nd:YAG laser for posterior capsulotomy and peripheral iridotomy.
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