GLIDESTAT Hydrophilic Guide Wire - Indonesia BPOM Medical Device Registration
GLIDESTAT Hydrophilic Guide Wire is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20501717473. The device is manufactured by UMBRA MEDICAL PRODUCTS, INC. from United States, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. MULTIDAYA MEDIKA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
UMBRA MEDICAL PRODUCTS, INC.Country of Origin
United States
Authorized Representative
PT. MULTIDAYA MEDIKAAR Address
RUKAN NIAGA GUNUNG SAHARI BLOK B-1
Registration Date
Apr 13, 2021
Expiry Date
Jan 01, 2024
Product Type
Diagnostic Cardiology Equipment
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