QUBE PRO Phacoemulsification System - Indonesia BPOM Medical Device Registration
QUBE PRO Phacoemulsification System is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21203420179. The device is manufactured by FRITZ RUCK OPTHALMOLOGISCHE SYSTEME GMBH from Germany, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is EAST RAYA LESTARI.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
FRITZ RUCK OPTHALMOLOGISCHE SYSTEME GMBHCountry of Origin
Germany
Authorized Representative
EAST RAYA LESTARIAR Address
Jl. Rawa Kepiting No. 4, Kawasan Industri Pulogadung
Registration Date
Aug 26, 2024
Expiry Date
Feb 01, 2029
Product Type
Surgical Eye Equipment
Phacofragmentation system.
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