POLYBIO - Indonesia BPOM Medical Device Registration
POLYBIO is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603020628. The device is manufactured by BIO SUD MEDICAL SYSTEMS S.R.L. from Italy, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. ALFA MEDICA BROTHERS.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
BIO SUD MEDICAL SYSTEMS S.R.L.Country of Origin
Italy
Authorized Representative
PT. ALFA MEDICA BROTHERSAR Address
Ruko Pondok Cabe Mutiara B/21
Registration Date
Oct 01, 2024
Expiry Date
Jul 30, 2029
Product Type
Surgical Equipment
Nonabsorbable poly(ethylene terephthalate) surgical suture.
Non Electromedic Sterile
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