H3-Check Complete - Indonesia BPOM Medical Device Registration
H3-Check Complete is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20208123266. The device is manufactured by ANALYTICON BIOTECHNOLOGIES AG. from Germany, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. BRIDGE TWO.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
ANALYTICON BIOTECHNOLOGIES AG.Country of Origin
Germany
Authorized Representative
PT. BRIDGE TWOAR Address
Petojo Melintang No. 17 Kel. Petojo Selatan, Kec. Gambir Jakarta Pusat
Registration Date
Jun 10, 2021
Expiry Date
Feb 04, 2024
Product Type
Hematological Reagents
Hematology quality control mixture.
Invitro Diagnostics
H3/5-Hypoclean
H3-Compact 500
H3-Compact 100
BIOLYZER FLUITEST GPT ALT
HEMOLYZER-5-Lyser
BIOLYZER TURBITEX CRP Latex
BIOLYZER FLUITEST GLU HK
HEMOLYZER 5 Control (L,N,H)
BIOLYZER CONTROPATH Plus
HEMOLYZER-5-Diff 5P
TECHNOCLONE AK-Calibrant
TECHNOCLONE MANUFACTURING OF DIAGNOSTICS AND PHARMACEUTICALS GMBH
TECHNOCLONE Coagulation Reference
TECHNOCLONE MANUFACTURING OF DIAGNOSTICS AND PHARMACEUTICALS LTD.,
TECHNOCLONE Coagulation Control A
TECHNOCLONE MANUFACTURING OF DIAGNOSTICS AND PHARMACEUTICALS LTD.
TC Thrombin Reagent
TECHNOCLONE MANUFACTURING OF DIAGNOSTICS AND PHARMACEUTICALS GMBH
ACTI-LANCE Lite Safety Lancet 28G
HTL-STREFA S.A.
TECHNOCLONE Fibrinogen Reagent Kit
TECHNOCLONE MANUFACTURING OF DIAGNOSTICS AND PHARMACEUTICALS GMBH
TC Coagulation Control AK
TECHNOCLONE MANUFACTURING OF DIAGNOSTICS AND PHARMACEUTICALS LTD.
TECHNOCHROM ATIII Kit
TECHNOCLONE MANUFACTURING OF DIAGNOSTICS AND PHARMACEUTICALS GMBH
EPIX Laparoscopic Grasper
APPLIED MEDICAL RESOURCES CORPORATION
MEDISAFE Solo, safety lancets
HTL-STREFA S.A.