CHIBA Biopsy Needle - Indonesia BPOM Medical Device Registration
CHIBA Biopsy Needle is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20504612059. The device is manufactured by ARGON MEDICAL DEVICES INC. from United States, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is PT. DIAN LANGGENG PRATAMA.
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Risk Classification
Product Class
Kelas : 3
Manufacturer
ARGON MEDICAL DEVICES INC.Country of Origin
United States
Authorized Representative
PT. DIAN LANGGENG PRATAMAAR Address
Jl. Raden Saleh Raya No. 4
Registration Date
Apr 24, 2020
Expiry Date
Jan 22, 2025
Product Type
Surgical Cardiology Equipment
Endomyocardial biopsy device.
Non Electromedic Sterile
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