AUTOCHECK Lancing Device - Indonesia BPOM Medical Device Registration
AUTOCHECK Lancing Device is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11603024453. The device is manufactured by I-SENS,INC from Korea, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. MEGA PRATAMA MEDICALINDO.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
I-SENS,INCCountry of Origin
Korea
Authorized Representative
PT. MEGA PRATAMA MEDICALINDOAR Address
Jl. Pluit Raya 133 Blok A.3
Registration Date
Apr 20, 2023
Expiry Date
Apr 16, 2026
Product Type
Surgical Equipment
Manual surgical instrument for general use.
Non Electromedic Non Sterile
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