FESCO Latex Foley Catheter (2 Ways) - Indonesia BPOM Medical Device Registration
FESCO Latex Foley Catheter (2 Ways) is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20805513970. The device is manufactured by WELL LEAD MEDICAL CO., LTD. from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. FESCO INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
WELL LEAD MEDICAL CO., LTD.Country of Origin
China
Authorized Representative
PT. FESCO INDONESIAAR Address
KOMP. RUKO MEGA GROSIR CEMPAKA MAS BLOK E 1, NO. 17, JL.LETJEN SOEPRAPTO , JAKARTA PUSAT, 10640
Registration Date
Jan 21, 2021
Expiry Date
Jan 21, 2024
Product Type
Therapeutic Gastroenterology-Urology Equipment
Urological catheter and accessories.
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