SHUNMEI Guiding Catheter - Indonesia BPOM Medical Device Registration
SHUNMEI Guiding Catheter is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20501220229. The device is manufactured by SHUNMEI 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
SHUNMEI 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
Jun 07, 2022
Expiry Date
Apr 16, 2024
Product Type
Diagnostic Cardiology Equipment
Percutaneous catheter.
Non Electromedic Sterile
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