AIM Filter - Indonesia BPOM Medical Device Registration
AIM Filter is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10203025904. The device is manufactured by GUANGZHOU LEIDE BIOSCIENCES CO., LTD. from China, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is FOKUS DIAGNOSTIC INDONESIA.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
GUANGZHOU LEIDE BIOSCIENCES CO., LTD.Country of Origin
China
Authorized Representative
FOKUS DIAGNOSTIC INDONESIAAR Address
Komp. Majapahit Permai Blok B No. 118 Jl. Majapahit Raya
Registration Date
Oct 06, 2020
Expiry Date
Dec 31, 2023
Product Type
Pathology Equipment and Accessories
Specimen transport and storage container.
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