BIOBASE Blood Bag Tube Sealer - Indonesia BPOM Medical Device Registration
BIOBASE Blood Bag Tube Sealer is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10209420480. The device is manufactured by BIOBASE BIODUSTRY (SHANDONG) CO., LTD. from China, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. PRIMASENTOSA CHRONICLE.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
BIOBASE BIODUSTRY (SHANDONG) CO., LTD.Country of Origin
China
Authorized Representative
PT. PRIMASENTOSA CHRONICLEAR Address
JL. RAYA JOGLO NO.19A JOGLO KEMBANGAN
Registration Date
Dec 16, 2024
Expiry Date
Oct 19, 2028
Product Type
Products used in the manufacture of blood preparations and preparations of origin and blood
Heat-sealing device.
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