TECHNOMED Balloon - Indonesia BPOM Medical Device Registration
TECHNOMED Balloon is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20505120538. 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 13, 2023
Expiry Date
Sep 18, 2028
Product Type
Therapeutic Cardiology Equipment
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