SANLI Vacuum Blood Collection Tubes for Single Use, Clot Activator - Indonesia BPOM Medical Device Registration
SANLI Vacuum Blood Collection Tubes for Single Use, Clot Activator is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101120585. The device is manufactured by LIUYANG SANLI MEDICAL TECHNOLOGY DEVELOPMENT CO., LTD. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. PYRIDAM FARMA.
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Risk Classification
Product Class
Kelas : 2
Country of Origin
China
Authorized Representative
PT. PYRIDAM FARMAAR Address
Ruko Villa Kebon Jeruk, Jl. Raya Kebon Jeruk Blok F3, Kel. Kebon Jeruk, Kec. Kebon Jeruk, Jakarta Barat, DKI Jakarta-11530
Registration Date
Jan 26, 2021
Expiry Date
Apr 01, 2025
Product Type
Clinical Chemistry Test System
Blood specimen collection device
Invitro Diagnostics
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