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“Conducted by a CMA/CNAS-accredited lab, our testing validates product safety and performance, providing credible quality assurance.”
Result: 8.01
Method: Disinfection Technical Specification (2002 Edition), Section 2.2.1.4
Arsenic (As): Not detected (<0.001 mg/L)
Cadmium (Cd): Not detected (<0.001 mg/L)
Mercury (Hg): Not detected (<0.0002 mg/L)
Lead (Pb): Not detected (<0.001 mg/L)
Method: Cosmetics Safety Technical Specification (2015 Edition), Chapter 4.1.6
Result: LC₅₀ > 10,000 mg/m³·BW
Conclusion: Practically non-toxic, compliant with Disinfection Technical Specification (2002 Edition) standards.
Result: LD₅₀ > 5,000 mg/kg·BW
Conclusion: Practically non-toxic, compliant with Disinfection Technical Specification (2002 Edition) standards.
Result: Non-irritating, meeting standard requirements.
Result: Irritation index 0 (Non-irritating).
Result: Irritation index 0 (Non-irritating).
Removal Rate: 94.2%
Test Method: GB/T 11742-1989, QB/T 2761-2006
Removal Rate: 90.4%
Test Method: QB/T 2761-2006
Test Standard: WS/T 650-2019 (5.2.1), comparable to EN 1276/EN 13697
Test Concentration: Undiluted product
Quantitative Suspension Test – 10-minute Exposure
Control: 4.1-4.4×10⁴ CFU/mL (avg. 4.2×10⁴ = 4.62 log₁₀)
Test: <10 CFU/mL (≤1.0 log₁₀)
➔ Log Reduction: ≥3.62 log₁₀
Control: 5.8-6.2×10⁴ CFU/mL (avg. 6.0×10⁴ = 4.78 log₁₀)
Test: <10 CFU/mL (≤1.0 log₁₀)
➔ Log Reduction: ≥3.78 log₁₀
Control: 3.4-4.4×10⁴ CFU/mL (avg. 3.8×10⁴ = 4.58 log₁₀)
Test: <10 CFU/mL (≤1.0 log₁₀)
➔ Log Reduction: ≥3.58 log₁₀
Control: 4.2-5.0×10⁴ CFU/mL (avg. 4.7×10⁴ = 4.67 log₁₀)
Test: 30-70 CFU/mL (1.48-1.85 log₁₀)
➔ Log Reduction: 2.82-3.19 log₁₀
Control: 3.8-4.3×10⁴ CFU/mL (avg. 4.1×10⁴ = 4.61 log₁₀)
Test: 50-60 CFU/mL (1.70-1.78 log₁₀)
➔ Log Reduction: 2.83-2.91 log₁₀
Control: 2.2-2.4×10⁴ CFU/mL (avg. 2.3×10⁴ = 4.36 log₁₀)
Test: <10 CFU/mL (≤1.0 log₁₀)
➔ Log Reduction: ≥3.36 log₁₀
Silver ion efficacy depends on usage conditions.
Quantitative Suspension Test – 15-minute Exposure
Control: 4.1-4.9×10⁴ CFU/mL (avg. 4.6×10⁴ = 4.66 log₁₀)
Test: <10 CFU/mL (≤1.0 log₁₀)
➔ Log Reduction: ≥3.66 log₁₀
Control: 5.2-5.7×10⁴ CFU/mL (avg. 5.4×10⁴ = 4.73 log₁₀)
Test: <10 CFU/mL (≤1.0 log₁₀)
➔ Log Reduction: ≥3.73 log₁₀
Control: 4.0-4.6×10⁴ CFU/mL (avg. 4.3×10⁴ = 4.63 log₁₀)
Test: <10 CFU/mL (≤1.0 log₁₀)
➔ Log Reduction: ≥3.63 log₁₀
Control: 5.1-5.8×10⁴ CFU/mL (avg. 5.5×10⁴ = 4.74 log₁₀)
Test: <10 CFU/mL (≤1.0 log₁₀)
➔ Log Reduction: ≥3.74 log₁₀
Silver ion efficacy depends on usage conditions.
Result: 8.01
Method: Disinfection Technical Specification (2002 Edition), Section 2.2.1.4
Arsenic (As): Not detected (<0.001 mg/L)
Cadmium (Cd): Not detected (<0.001 mg/L)
Mercury (Hg): Not detected (<0.0002 mg/L)
Lead (Pb): Not detected (<0.001 mg/L)
Method: Cosmetics Safety Technical Specification (2015 Edition), Chapter 4.1.6
Removal Rate: 94.2%
Test Method: GB/T 11742-1989, QB/T 2761-2006
Removal Rate: 90.4%
Test Method: QB/T 2761-2006
Control: 4.1-4.9×10⁴ CFU/mL (avg. 4.6×10⁴ = 4.66 log₁₀)
Test: <10 CFU/mL (≤1.0 log₁₀)
➔ Log Reduction: ≥3.66 log₁₀
Control: 5.2-5.7×10⁴ CFU/mL (avg. 5.4×10⁴ = 4.73 log₁₀)
Test: <10 CFU/mL (≤1.0 log₁₀)
➔ Log Reduction: ≥3.73 log₁₀
Control: 4.0-4.6×10⁴ CFU/mL (avg. 4.3×10⁴ = 4.63 log₁₀)
Test: <10 CFU/mL (≤1.0 log₁₀)
➔ Log Reduction: ≥3.63 log₁₀
Control: 5.1-5.8×10⁴ CFU/mL (avg. 5.5×10⁴ = 4.74 log₁₀)
Test: <10 CFU/mL (≤1.0 log₁₀)
➔ Log Reduction: ≥3.74 log₁₀
Silver ion efficacy depends on usage conditions.
Result: LC₅₀ > 10,000 mg/m³·BW
Conclusion: Practically non-toxic, compliant with Disinfection Technical Specification (2002 Edition) standards.
Result: LD₅₀ > 5,000 mg/kg·BW
Conclusion: Practically non-toxic, compliant with Disinfection Technical Specification (2002 Edition) standards.
Result: Non-irritating, meeting standard requirements.
Result: Irritation index 0 (Non-irritating).
Result: Irritation index 0 (Non-irritating).
Test Standard: WS/T 650-2019 (5.2.1), comparable to EN 1276/EN 13697
Test Concentration: Undiluted product
Quantitative Suspension Test – 10-minute Exposure
Control: 4.1-4.4×10⁴ CFU/mL (avg. 4.2×10⁴ = 4.62 log₁₀)
Test: <10 CFU/mL (≤1.0 log₁₀)
➔ Log Reduction: ≥3.62 log₁₀
Control: 5.8-6.2×10⁴ CFU/mL (avg. 6.0×10⁴ = 4.78 log₁₀)
Test: <10 CFU/mL (≤1.0 log₁₀)
➔ Log Reduction: ≥3.78 log₁₀
Control: 3.4-4.4×10⁴ CFU/mL (avg. 3.8×10⁴ = 4.58 log₁₀)
Test: <10 CFU/mL (≤1.0 log₁₀)
➔ Log Reduction: ≥3.58 log₁₀
Control: 4.2-5.0×10⁴ CFU/mL (avg. 4.7×10⁴ = 4.67 log₁₀)
Test: 30-70 CFU/mL (1.48-1.85 log₁₀)
➔ Log Reduction: 2.82-3.19 log₁₀
Control: 3.8-4.3×10⁴ CFU/mL (avg. 4.1×10⁴ = 4.61 log₁₀)
Test: 50-60 CFU/mL (1.70-1.78 log₁₀)
➔ Log Reduction: 2.83-2.91 log₁₀
Control: 2.2-2.4×10⁴ CFU/mL (avg. 2.3×10⁴ = 4.36 log₁₀)
Test: <10 CFU/mL (≤1.0 log₁₀)
➔ Log Reduction: ≥3.36 log₁₀
Silver ion efficacy depends on usage conditions.
“The biological efficacy test reports displayed on this page (e.g., for antimicrobial activity, deodorization) are provided for informational and educational purposes only. They document specific laboratory experiments conducted on solutions generated by the Argentumix device under controlled, standardized conditions as of the test date.”
PLEASE READ THIS CRITICAL NOTICE:
Not an Efficacy Claim: Our device is designed to generate a silver-ion solution for general hygiene and cleaning purposes. The test data is not intended to make any public health claim, and it does not establish that the generated solution is a registered or approved disinfectant, sanitizer, or antimicrobial pesticide under the regulations of the National Health Commission of the People’s Republic of China, the US EPA, or any other global health authority.
Laboratory Conditions vs. Real World: The results are strictly confined to the specific laboratory environment and methodology (e.g., GB/T 38497, ISO 22196) in which they were obtained. These conditions do not represent real-world use environments. Actual results in home or commercial settings will vary and are not guaranteed.
Not a Medical Device: Our product and the solution it generates are not medical devices and are not intended to diagnose, treat, mitigate, or prevent any disease.
For Authoritative Guidance:
✓ Consult the official regulations of your local health authority (e.g., NHC, FDA, EPA).
✓ Contact your legal counsel for definitive guidance on product classification and marketing claims.
Verification:
Full test reports are available for review upon request at
