LIATEST CONTROL N+P - Indonesia BPOM Medical Device Registration
LIATEST CONTROL N+P is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20208711440. The device is manufactured by DIAGNOSTICA STAGO SAS. from France, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. PROSPEROUS ADVANCED ERA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
DIAGNOSTICA STAGO SAS.Country of Origin
France
Authorized Representative
PT. PROSPEROUS ADVANCED ERAAR Address
Ruko Puri Botanical Junction Blok H7 / 17 Rt.007/01 Jl.Raya Joglo Kembangan - Jakarta Barat
Registration Date
Sep 10, 2021
Expiry Date
Mar 19, 2026
Product Type
Hematological Reagents
Hematology quality control mixture.
Invitro Diagnostics
STA System Control N+P
STA-PTT A 5
STACLOT DRVV Confirm
STACLOT DRVV Screen 2
STA Cleaner Solution
STA Staclot Protein S
STUBBORN OWREN-KOLLER
STA STACHROM Protein C
STA Stachrom AT III 3
STA Immunodef IX
STAGO sthemO PT M
DIAGNOSTICA STAGO S.A.S
STAGO sthemO VWF Cal
DIAGNOSTICA STAGO S.A.S
STHEMO Thrombin M
DIAGNOSTICA STAGO S.A.S
STAGO sthemO Unical
DIAGNOSTICA STAGO S.A.S
SD lnnovation TA-4V Aggregometer
SD INNOVATION S.A.S
STAGO sthemO CaCl2 M
DIAGNOSTICA STAGO S.A.S
STHEMO PTT A
DIAGNOSTICA STAGO S.A.S
sthemO Fib M
DIAGNOSTICA STAGO S.A.S
Stago Themo Oren Kaler M
DIAGNOSTICA STAGO S.A.S
FLUIDIL
SEBIA