EYEOP-PACK - Indonesia BPOM Medical Device Registration
EYEOP-PACK is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21203420180. The device is manufactured by EYE TECH CARE from France, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is RXILIENT MEDICAL INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
EYE TECH CARECountry of Origin
France
Authorized Representative
RXILIENT MEDICAL INDONESIAAR Address
Jalan Rawa Gelam V Blok L Kaveling 11-13, Kawasan Industri Pulo Gadung
Registration Date
Aug 27, 2024
Expiry Date
Apr 10, 2029
Product Type
Surgical Eye Equipment
Vitreous aspiration and cutting instrument.
Non Electromedic Sterile

