HEALAFLOW - Indonesia BPOM Medical Device Registration
HEALAFLOW is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 31203420036. The device is manufactured by BIO-STERIL SAS from France, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is PT. TRANSMEDIC INDONESIA.
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Risk Classification
Product Class
Kelas : 3
Manufacturer
BIO-STERIL SASCountry of Origin
France
Authorized Representative
PT. TRANSMEDIC INDONESIAAR Address
PERKANTORAN MENARA ERA UNIT G-01, JL. SENEN RAYA NO. 135-137
Registration Date
Feb 06, 2024
Expiry Date
Sep 14, 2028
Product Type
Surgical Eye Equipment
Intraocular fluid.
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