TEST REPORT APPLICANT : NING BO BESTT ELECTRIC CO., LTD ADDRESS : NO.3 MAOSHENG ROAD, YUYAO DEVELOPMENT AREA, ZHEJIANG, CHINA

Transcription

1 PAGE: 1 of 12 TEST REPORT APPLICANT : NING BO BESTT ELECTRIC CO., LTD ADDRESS : NO.3 MAOSHENG ROAD, YUYAO DEVELOPMENT AREA, ZHEJIANG, CHINA SAMPLE DESCRIPTION : (1) BLACK PA66+30%GF (2) WHITE SILICONE (3) TRANSPARENT SILICONE (4) RED SILICONE (5) SILVERY STAINLESS STEEL 304 (6) BLACK PP (7) TRANSPARENT PP (8) BLUE PP (9) WHITE CERAMIC MAT (10) WHITE POM (11) SEMI-TRANSPARENT TELFON (12) SILVERY BRASS NICKEL PLATING (13) BLACK PETG (14) TRANSPARENT GLASS (15) WHITE CERAMIC CUP STYLE / ITEM NO. : N/A SAMPLE RECEIVED DATE : APR. 25, 2017; APR. 27, 2017; MAY 02, 2017; MAY 08, 2017; MAY 22, 2017; MAY 27, 2017 TEST PERIOD : APR. 26, 2017 TO MAY 29, 2017 RESULT SUMMARY : PLEASE REFER TO NEXT PAGE(S). ********************FOR FURTHER DETAILS, PLEASE REFER TO THE FOLLOWING PAGE(S)****************** SIGNED FOR AND ON BEHALF OF EUROFINS TESTING TECHNOLOGY (SHENZHEN) CO. LTD. Harry Chen Lab & Technical Support Manager Coco Luo Lab & Reporting Manager Lydia Wang Lab Manager This test report is valid for the tested samples only. Without permission of the test center this test report is not permitted to be duplicated in extracts. This test report does not entitle to carry any safety mark on this or similar products.

2 PAGE: 2 of 12 RESULT SUMMARY : TEST(S) REQUESTED BY APPLICANT: RESULT - Maximum Extractable Fraction in Selected Solvents - US FDA 21 CFR PASS - Solubility in Boiling 4.2N HCl - US FDA 21 CFR PASS - Specific gravity and Melting point - US FDA 21 CFR PASS - Determining the amount of Net Chloroform Soluble Extractives - US FDA 21 CFR PASS - Total Chromium content in stainless steel - US FDA General Recognized As PASS Safe (GRAS) Specifications - Determining the amount of extractives - US FDA 21 CFR PASS - Density and Melting point - US FDA 21 CFR PASS - Maximum Extractable Fraction in Selected Solvents - US FDA 21 CFR PASS - Determining the amount of extractives - US FDA 21 CFR PASS Determining the amount of the total terephthaloyl moieties calculated as bis(2- hydroxyethyl terephthalate) - US FDA 21 CFR Determining the amount of The total terephthaloyl moieties calculated as cyclic trimer (C 6 H 4 CO 2 C 2 H 4 CO 2 ) 3 - US FDA 21 CFR PASS PASS - Inherent viscosity - US FDA 21 CFR PASS - Total Pb, As, Cd, Hg content - NSF/ANSI Food Equipment Materials Please refer to next page(s). - Determining the Net Chloroform soluble extractives - US FDA 21 CFR PASS - US FDA CPG Sec Pottery (Ceramics); Import and Domestic Lead Contamination. - US FDA CPG Sec Pottery (Ceramics); Import and Domestic Cadmium Contamination. PASS PASS

3 PAGE: 3 of 12 Material list Testing Component material No. 1 Black PA66+30%GF 2 White Silicone 3 Transparent Silicone 4 Red Silicone 5 Silvery Stainless steel Black PP 7 Transparent PP 8 Blue PP 9 White Ceramic Mat 10 White POM 11 Semi-transparent Telfon 12 Silvery Brass nickel plating 13 Black PETG 14 Transparent Glass 15 White Ceramic Cup Test Result: Maximum Extractable Fraction in Selected Solvents - US FDA 21 CFR Test method and limit with reference to US FDA 21 CFR Test Sample 1 Extractant (%) (%) (%) Water % Ethanol Ethyl Acetate Benzene N.D Note: - % = percentage by weight Solubility in Boiling 4.2N HCl - US FDA 21 CFR Test method and limit with reference to US FDA 21 CFR Test Sample 1 Solubility in Boiling 4.2N HC1 Dissolves in 1 hour Dissolves in 1 hour

4 PAGE: 4 of 12 Determining the amount of Net Chloroform Soluble Extractives - US FDA 21 CFR Test method and limit with reference to US FDA 21 CFR Test Sample 2 (mg/kg) (mg/kg) Extractant Test condition (mg/kg) Distilled water 30 minutes / 212 F N.D n-heptane 30 minutes / 120 F Note: - 1 mg/kg = 1 ppm = % - F = degrees Fahrenheit Total Chromium content in stainless steel - US FDA General Recognized As Safe (GRAS) Specifications Test method : Acid digestion followed by analysis with Inductively Coupled Argon Plasma Atomic Emission Spectrometry. Test Sample 5 (%) (%) Component (%) Total Chromium content Note: % = Percentage by weight - = greater than or equal to Determining the amount of extractives - US FDA 21 CFR Test method and limit with reference to US FDA 21 CFR Extractant Test Sample 6 8 Test condition (%) (%) (%) n-hexane Reflux temperature for 2 hours Xylene Dissolve the sample at 120 C and then cool at 25 C for 1 hours Test Sample 7 (%) (%) (%) Extractant Test condition (%) n-hexane Reflux temperature for 2 hours Xylene Dissolve the sample at 120 C and then cool at 25 C for 1 hours Note: - % = percentage by weight - C = degrees Celsius

5 PAGE: 5 of 12 Density and Melting point - US FDA 21 CFR Test method and limit with reference to US FDA 21 CFR Test Sample Density g/cm Melting point C Note: - g/cm 3 = gram per cubic centimeter - C = degrees Celsius Maximum Extractable Fraction in Selected Solvents - US FDA 21 CFR Test method and limit with reference to US FDA 21 CFR Test Sample 11 Test condition Test condition Distilled water Reflux temperature for 2 hours N.D % Ethanol Reflux temperature for 2 hours N.D Ethyl Acetate Reflux temperature for 2 hours N.D n-hexane Reflux temperature for 2 hours N.D Note: - mg/inch2 = milligram per square inch Determining the amount of extractives - US FDA 21 CFR Test method and limit with reference to US FDA 21 CFR Extractant Distilled water Test Sample 3 4 Test condition Test result Test result Reflux temperature for 7 hours Succeeding 2 hours of extraction N.D Note: - mg/inch 2 = milligram per square inch

6 PAGE: 6 of 12 Determining the amount of the total terephthaloyl moieties calculated as bis(2- hydroxyethyl terephthalate) - US FDA 21 CFR (#) Test method and limit with reference to US FDA 21 CFR Test Sample 13 Extractant Test condition (μg/cm 2 ) (μg/cm 2 ) Distilled water extracted with water added at 180 F and allowed to cool to 120 F 3% Acetic acid extracted with 3 percent(by volume) aqueous acetic acid added at 180 F and allowed to cool to 120 F 25% ethanol extracted for 24 hours with 25 percent (by volume) aqueous ethanol at 120 F Note: - F = degrees Fahrenheit - = less than or equal - mg/cm 2 = milligram per square centimeter (μg/cm 2 ) N.D N.D N.D Determining the amount of the total terephthaloyl moieties calculated as cyclic trimer (C 6 H 4 CO 2 C 2 H 4 CO 2 ) 3 - US FDA 21 CFR (#) Test method and limit with reference to US FDA 21 CFR Test Sample 13 Extractant Test condition (μg/cm 2 ) (μg/cm 2 ) n-heptane extracted for 2 hours with n-heptane at 120 F Note: - F = degrees Fahrenheit - = less than or equal - mg/cm 2 = milligram per square centimeter (μg/cm 2 ) N.D Inherent viscosity - US FDA 21 CFR (#) Test method and limit with reference to US FDA 21 CFR Component Test Sample 13 Inherent viscosity Note: - = greater than or equal to - # The result was subcontracted to lab: C014.

7 PAGE: 7 of 12 Total Pb, As, Cd, Hg content Test method with reference to NSF/ANSI Food Equipment Materials. Test Material No. 12 Parameter Unit Lead (Pb) mg/kg Arsenic (As) mg/kg N.D. 10 Cadmium (Cd) mg/kg N.D. 10 Mercury (Hg) mg/kg N.D. 10 Note: - 1 mg/kg = 1 ppm = % Determining the amount of Net Chloroform Soluble Extractives - US FDA 21 CFR Test method and limit with reference to US FDA 21 CFR Test Sample 10 Extractant Test condition Distilled water 30 minutes / 212 F N.D Note: - mg/inch 2 = milligram per square inch - F = degrees Fahrenheit

8 PAGE: 8 of 12 US FDA CPG Sec Pottery (Ceramics); Import and Domestic Lead Contamination Test method : AOAC methods Parameter Leachable of Lead content (Pb) Test Sample 9 Category (^) Unit limit 1 μg/ml N.D. N.D. N.D. N.D. N.D. N.D. 0.1 Parameter Leachable of Lead content (Pb) Test Sample 14 Category (^) Unit limit 3 μg/ml N.D. N.D. N.D. N.D. N.D. N.D. 0.1 Parameter Leachable of Lead content (Pb) Remark: Test Sample 15 Category (^) Unit (^) The permissible limit of leachable lead content is as follow: limit 2 μg/ml N.D. N.D. N.D. N.D. N.D. N.D. 0.1 No. Category Permissible of Lead extracted 1 Flatware 3.0 μg/ml 2 Small hollowware other than cups and mugs 2.0 μg/ml 3 Cups and mugs 0.5 μg/ml 4 Large hollowware other than pitchers 1.0 μg/ml 5 Pitchers 0.5 μg/ml

9 PAGE: 9 of 12 US FDA CPG Sec Pottery (Ceramics); Import and Domestic Cadmium Contamination Test method : AOAC methods Parameter Leachable of Cadmium content (Cd) Parameter Leachable of Cadmium content (Cd) Parameter Leachable of Cadmium content (Cd) Remark: Test Sample 9 Category (^) Unit limit 1 μg/ml N.D. N.D. N.D. N.D. N.D. N.D Test Sample 14 Category (^) Unit limit 2 μg/ml N.D. N.D. N.D. N.D. N.D. N.D Test Sample 15 Category (^) Unit limit 2 μg/ml N.D. N.D. N.D. N.D. N.D. N.D (^) The permissible limit of leachable cadmium content is as follow: No. Category Permissible of Cadmium extracted 1 Flatware 0.5 μg/ml 2 Small hollowware 0.5 μg/ml 3 Large hollowware 0.25 μg/ml Note: - μg/ml = microgram per milliliter

10 PAGE: 10 of 12 Other Information / Remark: (1)According to the customer s requirement, the appointed materials have been tested. (2) Replacement of report (No: EFSN C-C). Upon receipt of this report, the previous report (No: EFSN C-C) will be invalid immediately. Photo Attachment Material No. 1 Material No. 2 Material No. 3 Material No. 4 Material No. 5 Material No. 6

11 PAGE: 11 of 12 Photo Attachment Material No. 7 Material No. 8 Material No. 9 Material No. 10 Material No. 11 Material No. 12

12 PAGE: 12 of 12 Photo Attachment Material No. 13 Material No. 14 Material No. 15 The photos below are attached only for the customer s reference. ***END OF THE REPORT***