HEALON PRO sterile viscoelastic solution for intraocular use - Indonesia BPOM Medical Device Registration
HEALON PRO sterile viscoelastic solution for intraocular use is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 31203124875. The device is manufactured by AMO UPPSALA AB from Sweden, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is BRIDGE TWO.
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Risk Classification
Product Class
Kelas : 3
Manufacturer
AMO UPPSALA ABCountry of Origin
Sweden
Authorized Representative
BRIDGE TWOAR Address
Jl. Petojo Melintang No. 17
Registration Date
Nov 26, 2024
Expiry Date
May 28, 2029
Product Type
Surgical Eye Equipment
Intraocular fluid.
Non Electromedic Sterile
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