STREAMER™ Intracranial Balloon Dilation Catheter - Indonesia BPOM Medical Device Registration
STREAMER™ Intracranial Balloon Dilation Catheter is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 31003420120. The device is manufactured by BEIJING TAIJIEWEIYE TECHNOLOGY CO., LTD. from China, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is PT. CEKINDO BUSINESS INTERNATIONAL.
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Risk Classification
Product Class
Kelas : 3
Manufacturer
BEIJING TAIJIEWEIYE TECHNOLOGY CO., LTD.Country of Origin
China
Authorized Representative
PT. CEKINDO BUSINESS INTERNATIONALAR Address
CEKINDO BUSINESS INTERNATIONAL
Registration Date
Nov 13, 2024
Expiry Date
Aug 06, 2026
Product Type
Therapeutic Neurology Equipment
Intravascular occluding catheter.
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