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 21203810578. 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 PT. ANDAMAN MEDICAL INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
EYE TECH CARECountry of Origin
France
Authorized Representative
PT. ANDAMAN MEDICAL INDONESIAAR Address
Menara Cardig Lantai 1, Jalan Raya Halim Perdanakusuma
Registration Date
May 14, 2024
Expiry Date
Mar 23, 2028
Product Type
Surgical Eye Equipment
Vitreous aspiration and cutting instrument.
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