GP Care Latex Foley Catheter - Indonesia BPOM Medical Device Registration
GP Care Latex Foley Catheter is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20805026996. 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. GLOBAL PHARMA INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
WELL LEAD MEDICAL CO., LTD.Country of Origin
China
Authorized Representative
PT. GLOBAL PHARMA INDONESIAAR Address
PERGUDANGAN LIO BARU ASRI Jl. Bouraq Lio Baru Blok C1 No. 33 RT 004 RW 01, Batusari, Batuceper
Registration Date
Jul 11, 2023
Expiry Date
Sep 09, 2025
Product Type
Therapeutic Gastroenterology-Urology Equipment
Urological catheter and accessories.
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