KHOSLA Artificial Acrylic Eye - Indonesia BPOM Medical Device Registration
KHOSLA Artificial Acrylic Eye is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21202126518. The device is manufactured by KHOSLA SURGICAL INDUSTRIES from India, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. MEGA MEDICAL ABADI.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
KHOSLA SURGICAL INDUSTRIESCountry of Origin
India
Authorized Representative
PT. MEGA MEDICAL ABADIAR Address
Komplek Fatmawati Mas Blok B5 Kav. 207-208, Jl. RS. Fatmawati No. 20, RT. 005 RW. 010
Registration Date
Dec 18, 2023
Expiry Date
Nov 01, 2028
Product Type
Prosthetic Eye Equipment
Eye sphere implant.
Non Electromedic Non Sterile
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