SYNTHESIS PLUS Hydrophilic Preloaded IOL - Indonesia BPOM Medical Device Registration
SYNTHESIS PLUS Hydrophilic Preloaded IOL is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 31202320170. The device is manufactured by CUTTING EDGE SAS from France, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is SOCA MEDIKA INDONESIA.
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Risk Classification
Product Class
Kelas : 3
Manufacturer
CUTTING EDGE SASCountry of Origin
France
Authorized Representative
SOCA MEDIKA INDONESIAAR Address
Pulogadung Trade Center Blok 8 C No. 5, Jl. Raya Bekasi KM 21
Registration Date
Oct 04, 2023
Expiry Date
Dec 08, 2027
Product Type
Prosthetic Eye Equipment
Intraocular lens.
Non Electromedic Sterile

