WHEISMAN W-31D Diluent - Indonesia BPOM Medical Device Registration
WHEISMAN W-31D Diluent is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20208915545. 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. NOBLE BLESSINGS OF SIPOLIN.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
WHEISMAN MEDICAL TECHNOLOGY CO., LTDCountry of Origin
China
Authorized Representative
PT. NOBLE BLESSINGS OF SIPOLINAR Address
Jl. Limo Raya No. 2A RT.02 RW.01
Registration Date
Jul 04, 2024
Expiry Date
Mar 22, 2029
Product Type
Hematological Reagents
Blood cell diluents
Invitro Diagnostics
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