REXEED - Indonesia BPOM Medical Device Registration
REXEED is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20805900629. The device is manufactured by ASAHI KASEI MEDICAL MT., CORP. from Japan, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. KARYATAMA MANDIRI BUSINESS.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
ASAHI KASEI MEDICAL MT., CORP.Country of Origin
Japan
Authorized Representative
PT. KARYATAMA MANDIRI BUSINESSAR Address
Komplek Ruko D\'Best Blok B No. 39 Jl. RS Fatmawati No. 15 Gandaria Selatan
Registration Date
Jul 03, 2023
Expiry Date
Mar 29, 2026
Product Type
Therapeutic Gastroenterology-Urology Equipment
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