Product info
- Product name:Handheld biochemical immunoassay analyzer
- Product code:CCL-1601
Packaging Specifications
- Outer Packaging Size:0.21 × 0.09 × 0.06 m
- Gross Weight:0.75 kg
- Net Weight:0 kg
- Volume:0
Description
Handheld Biochemical Immunoassay Analyzer
PIONEERING IN HANDHELD POCT INSTRUMENTS
Device: Handheld Biochemical Immunoassay Analyzer
Principle: Dry Chemistry/Immunofluorescence
Sample Type: Whole blood, serum, plasma, urine, capillary blood, etc.
Weight: 750 g
Size: 210 mm (length) × 90 mm (width) × 60 mm (height)
Original Dual Methodology
Dry chemistry & Immunofluorescence
Result obtained in 0.5-15 min
Comprehensive Test Items
Covering 10+ diagnostic category
Up to 60+ test items
Exclusive & Featured Items
GLU/HbA1c Cre/MAU
AST/ALT FT3/FT4/TSH VD
Test Items List
Cardiovascular
- hs-cTnT: Sample Type P/WB, Time 10 min, Volume 80 μL, Detection Range 0.02-50 ng/mL, Methodology IF
- cTnT: Sample Type S, Time 10 min, Volume 80 μL, Detection Range 50-10000 pg/mL, Methodology IF
- cTnI/CK-MB/Myo: Sample Type S, Time 10 min, Volume 80 μL, Detection Range cTnI: 0.1-40 ng/mL; CK-MB: 2.5-80 ng/mL; Myo: 30-500 ng/mL, Methodology IF
- D-Dimer: Sample Type P/WB, Time 10 min, Volume 80 μL, Detection Range 0.1-10 μg/mL, Methodology IF
- NT-proBNP: Sample Type S, Time 10 min, Volume 80 μL, Detection Range 50-30000 pg/ml, Methodology IF
- MYO*: Sample Type S, Time 10 min, Volume 80 μL, Detection Range 30-600 ng/mL, Methodology IF
- cTnI/CK-MB*: Sample Type S, Time 10 min, Volume 80 μL, Detection Range CK-MB: 2.5-80 ng/mL; cTnI: 0.1-40 ng/mL, Methodology IF
- CK-MB*: Sample Type S, Time 10 min, Volume 80 μL, Detection Range 2.5-80 ng/mL, Methodology IF
- cTnT/NT-proBNP: Sample Type S, Time 10 min, Volume 80 μL, Detection Range cTnT: 50-10000 pg/mL; NT-proBNP: 50-30000 pg/mL, Methodology IF
- cTnI/NT-proBNP*: Sample Type S, Time 10 min, Volume 80 μL, Detection Range cTnI: 0.1-40 ng/mL; NT-proBNP: 50-30000 pg/mL, Methodology IF
- BNP*: Sample Type S, Time 10 min, Volume 80 μL, Detection Range 5-5000 pg/mL, Methodology IF
Inflammation
- Hs-CRP+CRP: Sample Type S/P/WB/CB, Time 3 min, Volume 5 μL, Detection Range CRP: 0.5-200 mg/L, Methodology IF
- PCT: Sample Type S, Time 10 min, Volume 80 μL, Detection Range 0.1-100 ng/mL, Methodology IF
- SAA/CRP: Sample Type S/P/WB/CB, Time 5 min, Volume 5 μL, Detection Range CRP: 0.5-200 mg/L; SAA: 3-200 mg/L, Methodology IF
- PCT/IL-6: Sample Type S, Time 10 min, Volume 80 μL, Detection Range PCT: 0.1-100 ng/mL; IL-6: 5-4000 pg/mL, Methodology IF
Thyroid Function
- FT3: Sample Type S/P/WB/CB, Time 10 min, Volume 50 μL, Detection Range 1.5-50 pmol/L, Methodology IF
- FT4: Sample Type S/P/WB/CB, Time 10 min, Volume 50 μL, Detection Range 6.4-77.2 pmol/L, Methodology IF
- TSH: Sample Type S/P/WB/CB, Time 10 min, Volume 50 μL, Detection Range 0.1-100 μIU/mL, Methodology IF
- FT3/FT4/TSH Combo: Sample Type S/CB; P/WB(EDTA), Time 15 min, Volume 50 μL, Detection Range TSH: 0.1-100 μIU/mL; FT4: 6.4-77.2 pmol/L; FT3: 1.5-50 pmol/L, Methodology IF
- T3: Sample Type S, Time 10 min, Volume 50 μL, Detection Range 0.5-10 nmol/L, Methodology IF
- T4: Sample Type S, Time 10 min, Volume 50 μL, Detection Range 15-300 nmol/L, Methodology IF
Metabolism
- 25-OH-VD: Sample Type S/CB; P/WB(Hep/CIT), Time 15 min, Volume 20 μL, Detection Range 8-70 ng/mL, Methodology IF
- UA: Sample Type S/CB; P/WB(EDTA/Hep), Time 30s-3 min, Volume 20 μL, Detection Range 50-1190 μmol/L, Methodology DC
Kidney Function
- UA/Cre/Urea: Sample Type S/CB; P/WB(EDTA), Time 5 min, Volume 50 μL, Detection Range Urea: 0.9-35.7 mmol/L; Cre: 30-1500 μmol/L; UA: 50-1190 μmol/L, Methodology DC
- MAU: Sample Type U, Time 5 min, Volume 100 uL, Detection Range 5-200 mg/L, Methodology IF
- Cre/MAU(2 in 1): Sample Type U, Time 5 min, Volume 100 μL, Detection Range Cre: 0.8-30 mmol/L; MAU: 10-200 mg/L, Methodology DC&IF
- Cre: Sample Type S/CB; P/WB(EDTA/CIT), Time 5 min, Volume 30 μL, Detection Range 30-1500 μmol/L, Methodology DC
- CysC: Sample Type S, Time 5 min, Volume 5 μL, Detection Range 0.2-8 mg/L, Methodology IF
Liver Function
- ALT/AST: Sample Type S/CB; P/WB(CIT), Time 5 min, Volume 30 μL, Detection Range 4-1000 U/L, Methodology DC
- TB/DB/IDB**: Sample Type S, Time 3 min, Volume 30 μL, Detection Range TB: 1.7-461-7 μmol/L; DB: 0-462 μmol/L; IDB: 0-462 μmol/L, Methodology DC
- TP/GB/WB*: Sample Type S, Time 3 min, Volume 30 μL, Detection Range TP: 20-110 g/L; GB: 5-50 μmol/L; WB: 10-60 μmol/L, Methodology DC
- ALP**: Sample Type S, Time 5 min, Volume 20 μL, Detection Range 5-5000 U/L, Methodology DC
- GGT**: Sample Type S, Time 5 min, Volume 20 μL, Detection Range 3-750 U/L, Methodology DC
Pancreatic
- LIP/AMY**: Sample Type S, Time 5 min, Volume 40 μL, Detection Range LIP: 20-6000 U/L; AMY: 5-1000 U/L, Methodology DC
Diabetes
- GLU: Sample Type S/CB; P/WB(EDTA/Hep), Time 30s-3 min, Volume 20 μL, Detection Range 2-25 mmol/L, Methodology DC
- HbA1c: Sample Type CB; WB(EDTA/Hep), Time 5 min, Volume 10 μL, Detection Range 4-14 %, Methodology IF
- GLU/HbA1c(2 in 1): Sample Type CB; WB(EDTA/Hep), Time 5 min, Volume 20 μL, Detection Range Glu: 2-25 mmol/L; HbA1c: 4%-14%, Methodology DC&IF
- INS: Sample Type S/P/WB/CB, Time 15 min, Volume 20 μL, Detection Range 0.2-1000 μIU/mL, Methodology IF
Blood Lipids
- TG/HDL-C/TCH/LDL-C: Sample Type S/CB; P/WB(EDTA/Hep), Time 30s-3 min, Volume 40 μL, Detection Range TG: 0.5-6 mmol/L; HDL-C: 0.2-2.5 mmol/L; TCH: 2.5-10.5 mmol/L; LDL-C: 0.2-5 mmol/L, Methodology DC
- TCH: Sample Type S/CB; P/WB(EDTA/Hep), Time 30s-3 min, Volume 20 μL, Detection Range TCH: 2.5-10.5 mmol/L, Methodology DC
Fertility
- β-HCG: Sample Type S, Time 10 min, Volume 5 μL, Detection Range 5-10000 mIU/mL, Methodology IF
- PRL: Sample Type S, Time 10 min, Volume 50 μL, Detection Range 1-200 ng/mL, Methodology IF
- FSH: Sample Type S, Time 10 min, Volume 20 μL, Detection Range 1-100 mIU/mL, Methodology IF
- LH: Sample Type S, Time 10 min, Volume 50 μL, Detection Range 1-100 mIU/mL, Methodology IF
- AMH: Sample Type S, Time 10 min, Volume 50 μL, Detection Range 0.1-20 ng/mL, Methodology IF
- TES: Sample Type S, Time 10 min, Volume 50 μL, Detection Range 0.2-15 ng/mL, Methodology IF
- E2: Sample Type S, Time 15 min, Volume 20 μL, Detection Range 9-3000 pg/mL, Methodology IF
- Prog: Sample Type S, Time 10 min, Volume 80 μL, Detection Range 1.5-60 ng/mL, Methodology IF
Tumor Marker
- fPSA: Sample Type S, Time 10 min, Volume 50 μL, Detection Range 0.1-50 ng/mL, Methodology IF
- tPSA: Sample Type S, Time 15 min, Volume 10 μL, Detection Range 2-80 ng/mL, Methodology IF
- CEA*: Sample Type S, Time 10 min, Volume 20 μL, Detection Range 2-1000 ng/mL, Methodology IF
- AFP: Sample Type S, Time 10 min, Volume 50 μL, Detection Range 1-1000 ng/mL, Methodology IF
- FOB: Sample Type F, Time 5 min, Volume 50 mg, Detection Range 20-10000 ng/mL, Methodology IF
- CA-125: Sample Type S, Time 15 min, Volume 20 μL, Detection Range 2-500 U/mL, Methodology IF
- CA-242*: Sample Type S, Time 15 min, Volume 20 μL, Detection Range 2-500 U/mL, Methodology IF
- CA-50*: Sample Type S, Time 15 min, Volume 20 μL, Detection Range 2-500 U/mL, Methodology IF
- CA19-9: Sample Type S, Time 10 min, Volume 50 μL, Detection Range 2-500 U/mL, Methodology IF
- CA15-3*: Sample Type S, Time 15 min, Volume 20 μL, Detection Range 2-300 U/mL, Methodology IF
Digestive Diseases
- HP ag: Sample Type F, Time 10 min, Volume 50 mg, Detection Range 0.1-100 ng/mL, Methodology IF
- CAL: Sample Type F, Time 10 min, Volume 50 mg, Detection Range 20-1000 μg/g, Methodology IF
Infectious Disease
- anti-HCV: Sample Type S, Time 10 min, Volume 50 μL, Detection Range 1-1000 S/CO, Methodology IF
- Syphilis: Sample Type S, Time 15 min, Volume 100 μL, Detection Range 1-50 S/CO, Methodology IF
- HBsAg: Sample Type S, Time 10 min, Volume 80 μL, Detection Range 0.1-2000 IU/mL, Methodology IF
- Dengue NS1*: Sample Type S, Time 10 min, Volume 80 μL, Detection Range 0.5-1000 ng/mL, Methodology IF
- Dengue IgM/IgG*: Sample Type S, Time 10 min, Volume 80 μL, Detection Range 1-20 S/CO, Methodology IF
Anemia
- HB: Sample Type WB/CB, Time 1 min, Volume 5 μL, Detection Range 4.5-25.6 g/dL, Methodology DC
- Fer: Sample Type S, Time 10 min, Volume 50 μL, Detection Range 10-1000 ng/mL, Methodology IF
Trace elements
- Ca**: Sample Type S, Time 3 min, Volume 20 μL, Detection Range 0.25-3.49 μmol/L, Methodology DC
- Zn**: Sample Type S, Time 3 min, Volume 20 μL, Detection Range 0.61-115.21 μmol/L, Methodology DC
- P**: Sample Type S, Time 3 min, Volume 20 μL, Detection Range 0.3-6.0 mmol/L, Methodology DC
Other
- IgE: Sample Type S, Time 10 min, Volume 20 μL, Detection Range 5-1000 IU/mL, Methodology IF
- GLU/UA/TG/TCH: Sample Type S/CB; P/WB(EDTA/Hep), Time 30s-3 min, Volume 50 μL, Detection Range GLU: 2-25 mmol/L; UA: 50-1190 μmol/L; TG: 0.5-6 mmol/L; TCH: 2.5-10.5 mmol/L, Methodology DC
- Cor: Sample Type S, Time 10 min, Volume 80 μL, Detection Range 5-1000 nmol/L, Methodology IF
- *Coming Soon **In Development
- WB: Whole blood; S: Serum; P: Plasma; CB: capillary blood; U: Urine; F: Feces
- IF: Immunofluorescence; DC: Dry Chemistry
- EDTA: EDTA anticoagulant; Hep: Heparin anticoagulant; CIT: Citrated anticoagulant
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