BROSMED Balloon Inflation Device - Indonesia BPOM Medical Device Registration
BROSMED Balloon Inflation Device is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20501320998. 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. WIKATON MITRA TAMA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
BROSMED MEDICAL CO., LTD.Country of Origin
China
Authorized Representative
PT. WIKATON MITRA TAMAAR Address
GEDUNG TRIO,JL MAMPANG PRAPATAN RAYA NO.17 RT 004/006, KEL MAMPANG PRAPATAN KEC MAMPANG PRAPATAN
Registration Date
Sep 05, 2023
Expiry Date
Mar 01, 2026
Product Type
Diagnostic Cardiology Equipment
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