DELVI CARE 2 Way Latex Foley Catheter - Indonesia BPOM Medical Device Registration
DELVI CARE 2 Way Latex Foley Catheter is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20805022755. 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. SAFIRA DWI PHARMA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
WELL LEAD MEDICAL CO., LTD.Country of Origin
China
Authorized Representative
PT. SAFIRA DWI PHARMAAR Address
Perumahan Graha Harapan Blok E 14 No. 12 RT 005 RW 018
Registration Date
Mar 22, 2023
Expiry Date
Dec 01, 2024
Product Type
Therapeutic Gastroenterology-Urology Equipment
Urological catheter and accessories.
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