HANGZHOU FUSHAN PEG Kit - Indonesia BPOM Medical Device Registration
HANGZHOU FUSHAN PEG Kit is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20805420089. The device is manufactured by HANGZHOU FUSHAN MEDICAL APPLIANCES CO., LTD from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is INDOMAKMUR DWI LESTARI.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
HANGZHOU FUSHAN MEDICAL APPLIANCES CO., LTDCountry of Origin
China
Authorized Representative
INDOMAKMUR DWI LESTARIAR Address
Rukan Sedayu Square, Blok D No 10 Lantai 3
Registration Date
Feb 02, 2024
Expiry Date
Nov 12, 2028
Product Type
Therapeutic Gastroenterology-Urology Equipment
Gastrointestinal tube and accessories.
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