BALLAST 088 Long Sheath - Indonesia BPOM Medical Device Registration
BALLAST 088 Long Sheath is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20501321156. The device is manufactured by BALT USA, LLC from United States, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is MEDIKON MAIN PHARMALAB.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
BALT USA, LLCCountry of Origin
United States
Authorized Representative
MEDIKON MAIN PHARMALABAR Address
JLN. RAYA PASAR MINGGU NO 15, RT.001/07
Registration Date
Nov 17, 2023
Expiry Date
Dec 31, 2025
Product Type
Diagnostic Cardiology Equipment
Percutaneous catheter.
Non Electromedic Sterile
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