SAMMORA Lancet Device Plastic - Indonesia BPOM Medical Device Registration
SAMMORA Lancet Device Plastic is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11603021075. The device is manufactured by HANSOL MEDICAL CO., from Korea, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. SINTHE UTAMA INDONESIA.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
HANSOL MEDICAL CO.,Country of Origin
Korea
Authorized Representative
PT. SINTHE UTAMA INDONESIAAR Address
Jl. Semangat No. 73 B Rt.017/ Rw.011 Kelurahan Mangga Dua Selatan Kecamatan Sawah Besar
Registration Date
Feb 09, 2023
Expiry Date
Feb 08, 2026
Product Type
Surgical Equipment
Manual surgical instrument for general use.
Non Electromedic Non Sterile
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