FEROZE Latex Foley Catheter - Indonesia BPOM Medical Device Registration
FEROZE Latex Foley Catheter is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20805420312. 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. BUANA INTIPRIMA MEDIKA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
WELL LEAD MEDICAL CO., LTD.Country of Origin
China
Authorized Representative
PT. BUANA INTIPRIMA MEDIKAAR Address
Rukan Sentra Niaga Green Lake City Blok F No.3
Registration Date
Jun 12, 2024
Expiry Date
Jun 11, 2027
Product Type
Therapeutic Gastroenterology-Urology Equipment
Urological catheter and accessories.
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