STAGO sthemO VWF Ag - Indonesia BPOM Medical Device Registration
STAGO sthemO VWF Ag is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20207420181. The device is manufactured by DIAGNOSTICA STAGO S.A.S from France, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PROSPEROUS ADVANCED ERA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
DIAGNOSTICA STAGO S.A.SCountry of Origin
France
Authorized Representative
PROSPEROUS ADVANCED ERAAR Address
RUKO PURI BOTANICAL MEGA KEBON JERUK H.7 NO.17
Registration Date
Nov 09, 2024
Expiry Date
Dec 31, 2027
Product Type
Haematology Package and Kit
Factor deficiency test.
Invitro Diagnostics
STAGO sthemO PT M
STAGO sthemO VWF Cal
STHEMO Thrombin M
STAGO sthemO Unical
STHEMO PTT A
STHEMO CK PREST
STAGO sthemO CaCl2 M
sthemO Fib M
Stago Themo Oren Kaler M
STHEMO CK PREST
DIAGNOSTICA STAGO S.A.S
CSF Control
SEBIA
HYDRAGEL 3 CSF ISOFOCUSING
SEBIA
HYDRAGEL 1 THINK JONES
SEBIA
CAPILLARYS 3 WASH SOLUTION
SEBIA
CAPICLEAN
SEBIA
STA Unicalibrator
DIAGNOSTICA STAGO S.A.S.