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 20805321092. 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
RUKO MEGA GROSIR CEMPAKA MAS BLOK E 1/17 Jalan Letjend Suprapto Rt 07 Rw 08, Prov. DKI Jakarta, Kota Jakarta Pusat, Kec. Kemayoran, Kel. Sumur Batu
Registration Date
Dec 29, 2023
Expiry Date
Dec 28, 2026
Product Type
Therapeutic Gastroenterology-Urology Equipment
Urological catheter and accessories.
Non Electromedic Sterile
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