EndoVive Standard Balloon Replacement Kit - Indonesia BPOM Medical Device Registration
EndoVive Standard Balloon Replacement Kit is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20805912757. The device is manufactured by XERIDIEM MEDICAL DEVICES from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is BOSTON SCIENTIFIC INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
XERIDIEM MEDICAL DEVICESCountry of Origin
United States
Authorized Representative
BOSTON SCIENTIFIC INDONESIAAR Address
Prudential Tower lantai 28 Jl. Jend. Sudirman Kav. 79
Registration Date
Dec 30, 2022
Expiry Date
Apr 20, 2027
Product Type
Therapeutic Gastroenterology-Urology Equipment
Gastrointestinal tube and accessories.
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