HUMAN LDH SCE Mod. LiquiUV - Indonesia BPOM Medical Device Registration
HUMAN LDH SCE Mod. LiquiUV is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101803339. The device is manufactured by HUMAN GESELLSCHAFT FOR BIOCHEMICA UND DIAGNOSTICA MBH. from Germany, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is SALI POLAPA TOGETHER.
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Risk Classification
Product Class
Kelas : 2
Country of Origin
Germany
Authorized Representative
SALI POLAPA TOGETHERAR Address
Puri Sentra Niaga Blok B 33-34 Jl. Raya Kalimalang 13620
Registration Date
Apr 03, 2023
Expiry Date
Dec 31, 2027
Product Type
Clinical Chemistry Test System
Lactate dehydrogenase test system (kit & cair)
Invitro Diagnostics
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