WHEISMAN Hematology Control - Indonesia BPOM Medical Device Registration
WHEISMAN Hematology Control is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20208320793. The device is manufactured by WHEISMAN MEDICAL TECHNOLOGY CO., LTD. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. LIFOTRONIC TECHNOLOGY INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
WHEISMAN MEDICAL TECHNOLOGY CO., LTD.Country of Origin
China
Authorized Representative
PT. LIFOTRONIC TECHNOLOGY INDONESIAAR Address
Ruko South Goldfinch Blok SGA No. 17, Jl. Spring Boulevard, Kode Pos 15322, Kel. Cihuni, Kec. Pagedangan, Kab. Tangerang, Provinsi Banten
Registration Date
Oct 23, 2023
Expiry Date
Jul 10, 2028
Product Type
Hematological Reagents
Hematology quality control mixture.
Invitro Diagnostics
WHEISMAN Hematology Control
WHEISMAN MEDICAL TECHNOLOGY CO., LTD.
WHEISMAN Hematology Control
WHEISMAN MEDICAL TECHNOLOGY CO. LTD.
WHEISMAN Hematology Control
WHEISMAN MEDICAL TECHNOLOGY CO., LTD.
WHEISMAN Hematology Control
WHEISMAN MEDICAL TECHNOLOGY CO. LTD.
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WHEISMAN Hematology Control
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