SURGICATH Latex Foley Catheter 2 Way Standard - Indonesia BPOM Medical Device Registration
SURGICATH Latex Foley Catheter 2 Way Standard is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20805122188. 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. KARINDO ALKESTRON.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
WELL LEAD MEDICAL CO., LTD.Country of Origin
China
Authorized Representative
PT. KARINDO ALKESTRONAR Address
JL. TOMANG RAYA NO.17
Registration Date
Feb 22, 2024
Expiry Date
Feb 21, 2027
Product Type
Therapeutic Gastroenterology-Urology Equipment
Urological catheter and accessories.
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