MKCELLS A.V. Fistula Needle Sets - Indonesia BPOM Medical Device Registration
MKCELLS A.V. Fistula Needle Sets is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20805420299. The device is manufactured by SHANDONG WEIGAO BLOOD PURIFICATION PRODUCTS CO., LTD. from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. INTERSKALA SEHAT SEJAHTERA.
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Risk Classification
Product Class
Kelas : 2
Country of Origin
China
Authorized Representative
PT. INTERSKALA SEHAT SEJAHTERAAR Address
INTERSKALA SEHAT SEJAHTERA
Registration Date
Jun 06, 2024
Expiry Date
Jun 04, 2027
Product Type
Therapeutic Gastroenterology-Urology Equipment
Blood access device and accessories.
Non Electromedic Sterile
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