TECHNOMED Guide Wire GWC - Indonesia BPOM Medical Device Registration
TECHNOMED Guide Wire GWC is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20501120529. The device is manufactured by BROSMED MEDICAL CO., LTD. from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. TRIPUTRA TECHNO MED.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
BROSMED MEDICAL CO., LTD.Country of Origin
China
Authorized Representative
PT. TRIPUTRA TECHNO MEDAR Address
Jl. Metro Tanjung Bunga Ruko Sumba Opu Blok A/17
Registration Date
Dec 14, 2023
Expiry Date
Dec 13, 2026
Product Type
Diagnostic Cardiology Equipment
Catheter guide wire.
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