STARIS LIFT PDO Mold - Indonesia BPOM Medical Device Registration
STARIS LIFT PDO Mold is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603324329. The device is manufactured by 2L BIO CO., LTD. from Korea, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. HAJU MEDICAL INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
2L BIO CO., LTD.Country of Origin
Korea
Authorized Representative
PT. HAJU MEDICAL INDONESIAAR Address
Gedung Tifa Arum Realty Lt.8, Suite 801 Jl. Kuningan Barat 1 No. 26, Kelurahan Kuningan Barat, Kecamatan Mampang Prapatan. Jakarta Selatan, DKI Jakarta
Registration Date
Aug 01, 2023
Expiry Date
Feb 14, 2028
Product Type
Surgical Equipment
Absorbable polydioxanone surgical suture.
Non Electromedic Sterile
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