ABLE Disposable Fistula Needle - Indonesia BPOM Medical Device Registration
ABLE Disposable Fistula Needle is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20805813819. The device is manufactured by GUANGDONG BAIHE MEDICAL TECHNOLOGY CO., LTD. from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. EUREKA ETERNAL SUCCESS.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
GUANGDONG BAIHE MEDICAL TECHNOLOGY CO., LTD.Country of Origin
China
Authorized Representative
PT. EUREKA ETERNAL SUCCESSAR Address
Jl. pantai Indah Barat Komplek Toho Blok B No. 21 Rt/Rw 001/003 Kelurahan Muara Kamal Kec. Penjaringan Jakarta Utara
Registration Date
Jun 29, 2022
Expiry Date
Mar 24, 2027
Product Type
Therapeutic Gastroenterology-Urology Equipment
Blood access device and accessories.
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