DA:ALL I-Screw - Indonesia BPOM Medical Device Registration
DA:ALL I-Screw is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603422848. The device is manufactured by META BIOMED CO., LTD. from Korea, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. ANAYA ADHI KENCANA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
META BIOMED CO., LTD.Country of Origin
Korea
Authorized Representative
PT. ANAYA ADHI KENCANAAR Address
Foresta Business Loft 7 No 8, Jalan BSD Boulevard Utara
Registration Date
Dec 13, 2024
Expiry Date
May 08, 2029
Product Type
Surgical Equipment
Absorbable polydioxanone surgical suture.
Non Electromedic Sterile
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