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1. Test Report No. T 11434 - 01 Issue 1 NIOSH TEB - APR - STP - 0039A: Formaldehyde Service Life BLS srl BLS Model s 242 ABE2 & 243 ABEK2 Respirator Cartridges 3 March 2017 Authorized and Reviewed by: Performed by: Michael G. Gergel Prabodh K . Patnaik Manager – Physical & Analytical Chemistry Physical / Analytical Scientist a) Reports are issued pursuant to the ICS standard Terms and Conditions agreement. b) The contents of this test r eport are confidential. Reproduction of the report is prohibited except in full, unless approved in writing by ICS Laboratories, Inc. c) Unless otherwise indicated, the test results contained in this report apply only to the samples tested and not to lot s or batches from which they were taken. d) Where applicable, test data provided by subcontractor is uniquely identified in the test report. e) Where applicable, test data not covered under our ISO/IEC 17025 Accreditation is uniquely identified in the te st report. WARNING: This Test Report may contain technical data whose export is restricted by the Arms Export Control Act (Title 22, U.S . C., Sec 2751, et seq.) or the Export Administration Act of 1979, as amended, Title 50, U.S.C., App. 2401 et seq. and which may not be exported, released or disclosed to non - U.S. persons (i.e. persons who are not U.S. citizens or lawful permanent residents ["green card" holders]) inside or outside the United States, without first obtaining an export license. Violations o f these export laws are subject to severe civil, criminal and administrative penalties. ICS Laboratories, Inc. ●1072 Industrial Parkway North ● Brunswick, Ohio 44212 USA Phone: 330.220.0515 Fax: 330.220.0516

4. Issued to: BLS srl. Date : 3 March 2017 Via Dei Giovi, 41 Report: T11434 - 01 20032 Cormano (MI) Issue: 1 Italy Page: 3 of 3 Photographs: Figure 1: BLS respirator cartridges \ Figure 2: Formaldehyde service life in progress

5. TERMS AND CONDITIONS 1. Client acknowledges that ICS Laboratories (ICS) performs testing services only as specified by Client. ICS does not design, warrant, supervise or monitor compliance of products or services except as specifically agreed to in writing. By their very nature , testing, analysis, and other ICS services are limited in scope and subject to expected measurement variability. 2. Client or Client’s authorized representative shall be afforded the opportunity to clarify test requests and reasonable access to monitor test work, provisional to protecting the confidentiality of other clients. 3. ICS shall keep documents and information related to Client confidential and will not disclose any such inform ation to third parties without C lient permission. ICS will, however, disclos e any such information in response to compulsory legal process after providing Client with a copy of such process. 4. ICS Reports apply only to the standards or procedures identified therein and to the sample (s) tested and or inspection (s) made. Test and/o r inspection results are not indicative or representative of the qualities of the lot from which the sample was taken or of apparently identical or similar products. 5. ICS Test Reports and their insignia ar e for the exclusive use of the C lient. Reports, in their entirety, may b e utilized at the discretion of Clients and/or their authorized agents for purposes including, but not limited to, research & development, recordkeeping, product packaging, educat ional and promotional mater ials in various formats, cert ification, and compliance. As an accredited independent testing laboratory, ICS maintains an interest in preventing the misrepresentation of the contents of its test re ports. As such, C lients may NOT use, reproduce or otherwise disseminate excerpted, par tial, redacted or otherwise altered ICS test reports without the prior review of such use by ICS and the granting of its written approval. Further, Client s are prohibited from manipulating data and/or extrapolating - from - it statistics or conclusions that c ontradict or eclipse the empirical results of testing as reflected by the totality of the report. Client s are to refrain from utilizing ICS Test Reports and/or the ICS logo in a manner t hat suggests any extra - report conclusions are provided and/or endorsed by ICS Laboratories. 6. Any use by Client of ICS’s Reports or the information contained therein is conditioned on timely payment of all fees. 7. The name (s) listed as the “Issued to” party on test reports may not reflect the actual entity submitting and/or cont racting the assessment. 8. 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Client agrees to pay any and all additional costs associated with unexpected or above - standard communicat ions and/or consultations with C lient or third parties as designated by C lient. 17. Client agrees to pay any and all additional costs for work additional to the original scope of work as agreed to by C lient. 18. Client understands and agrees that ICS, in entering into this Contract and by performing services hereunder, does not assume, abridge, abrogate or undertake to discharge any duty or responsibility of Client to any other party or pa rties. No one other than Client shall have any right to rely on any Report or other representation of conduct of ICS and ICS disclaims any obligations of any nature whatsoever with respect to such person. 19. Client agrees, in consideration of ICS undertaking to perform the test(s) hereunder, to protect , defend and indemnify ICS from any and all claims, damages, expenses either direct or consequential for injuries to persons or property arising out of or in consequence of the performance of the testing, inspec tion and reporting hereunder and/or the performance of the products tested or inspected hereunder , UNLESS CAUSED BY THE NEGLIGENCE OF ICS. 20. IT IS AGREED THAT IF ICS SHOULD BE FOUND LIABLE FOR ANY LOSSES OR DAMAGES ATTRIBUTABLE TO THE SERVICES HEREUNDER IN A NY RESPECT, ITS LIABILITY SHALL IN NO EVENT EXCEED THE AMOUNT OF THE FEE PAID BY CLIENT FOR SUCH SERVICES AND CLIENT’S SOLE REMEDY AT LAW OR IN EQUITY SHALL BE THE RIGHT TO RECOVER UP TO SUCH AMOUNT. 21. Quotations are valid for 30 days from date of issue. Te rms: 30% Laboratory/Testing fees invoiced and payable upon acceptance of quotation. Remaining fees invoiced and payable upon completion of services, 15 days net. Cancelled jobs will be invoiced for work performed and/or set - up costs incurred. Cancelled Purchase Orders are subject to 10% service charge. Shipping costs incurred by ICS will be invoic ed at cost +10% handling fee. A minimum USD $25.00 handling fee will be also invoiced. For shipping costs incurred by C lient, ICS will invoice a minimum USD $ 25.00 handling fee. 22. In the event that payment is not received within 15 days of invoice date, Client agrees to pay a late payment charge on the unpaid balance equal to 1 - 1/2% per month or the maximum charge allowed by law, whichever is less, and all costs and expenses, including attorney’s fees where recovery of the same is not prohibited by law, incurred by ICS in collecting such invoices. 23. All costs associated with compliance with any subpoena (s) for documents, testimony in a court of law, or for any othe r purpose relating to work performed by ICS in connection with work performed for that Client, shall be paid by Client. Client shall also pay ICS’s then existing standard fee for consulting, deposition and trial testimony and all expenses related thereto. 24. Cancelled/discontinued orders: Client responsible for all administrative and testing char ges up to point of cancellation . ICS Laboratories, Inc. · 1072 Industrial Parkway North · Brunswick · Ohio · 44212 · USA AF 1.4 - 03 (12 Dec 14)

3. Issued to: BLS srl. Date : 3 March 2017 Via Dei Giovi, 41 Report: T11434 - 01 20032 Cormano (MI) Issue: 1 Italy Page: 2 of 3 Results: The physical measurements and formaldehyde service - life results for the cartridges are summarized below. Table I Physical Measurements for filter s tested against Formaldehyde Cartridge ID Initial Weight (g ) Initial Resistance (mm . H 2 O @ 85 LPM) Conditioned Weight (g) Final Weight (g) Final Resistance (mm. H 2 O @ 85 LPM) Inhalation Exhalation Inhalation Exhalation 1 121.4 21.6 20.9 AR 125.0 21.1 23.0 2 135.8 AR 137.4 3 120.3 20.2 19.9 AR 124.9 19.9 21.7 4 136.4 AR 138 .0 5 121.3 21.1 20.8 AR 126.0 20.5 22.1 6 138.4 AR 140.1 7 121.2 19.0 18.2 124.1 123.7 18.2 19.4 8 129.8 129.0 128.2 9 119.0 19.3 18.9 121.1 121.3 18.7 20.3 10 133.5 131.2 131.6 11 120.3 19.5 19.3 136.4 131.1 18.5 20.1 12 137.6 151. 6 145.2 13 121.4 19.8 19.4 138.1 135.6 19.4 20.7 14 132.9 148.1 144.9 Table II Service Life Results for filter s tested against Formaldehyde Filter No. Filter Conditioning RH (%) Test Condition HCHO Conc. (ppm) Down - stream Temp. (º C) NIOSH BT spec. Measured BT Conc. (ppm) Measured BT Time (min) Result Airflow (LPM) RH (%) Temp. (25 o C) Conc. (ppm) Time (min) 1, 2 AR 64 50 25 100 26.0 1.0 50 0.14 60 Pass 3 , 4 AR 64 50 25 100 26.0 0.16 60 Pass 5 , 6 AR 64 50 25 10 0 25.6 0.04 60 Pass 7 , 8 25 64 25 25 100 23.7 0.06 60 Pass 9 , 10 25 64 25 25 100 23.9 0.01 60 Pass 11 , 12 85 64 85 25 100 31.0 0.03 60 Pass 13 , 14 85 64 85 25 100 30.5 0.17 60 Pass

2. Issued to: BLS srl. Date : 3 March 2017 Via Dei Giovi, 41 Report: T11434 - 01 20032 Cormano (MI) Issue: 1 Italy Page: 1 of 3 Summary: Two models of A BE2 filters for a twin - cartridge a ir p urifying half - mask r espirator were evaluated for formaldehyde service li fe in accordance with NIOSH Procedure RCT - APR - STP - 00 39A . The samples were submitted by BLS srl. All samples met the requ irement , as specified in the standard. Objective: Testing to: NIOSH TEB - APR - STP - 0039A : “Determination of Formaldehyde Service Life Test, Air Purifying Respirators with Cartridges Standard Testing Procedure” Revision: 2.0 Date: 1December 2008 M aterials: Sample ID . Description Quantity BLS 2 42 BLS 2 42 ABE 2 Filter cartridge for twin cartridge h alf - m ask respirator 16 BLS 243 BLS 243 ABEK 2 Filter cartridge for twin cartridge half - mask respirator 16 - Cartridge adapter, Bayonet mount 2 Date provided by the Client: 16 December 201 6 Date Testing Authorized: 5 January 2017 Dates of tests: 27 February - 2 March 2017 Manufacturer / Supplier: BLS srl Equipments and Reagents: Miller Nelson Humidity Control Systems , HC S - 401 (EQ0380) Digital Balance , Acculab V - 600 (EQ0112) Syringe Pump (EQ0360) Test Chamber , 13” x 9” x 18”, custom designed Digital Thermometer , (EQ0325) Vaisala Humidity and Temperature Indicators (EQ030 7 & EQ030 8 ) Electronic Timer , Co ntrol Company (EQ 1150 - 11 ) Custom Test bench for Inhalation and Exhalation Resistance Formaldehyde Gas Analyzer , Interscan Corp. (EQ0429) Formaldehyde, 37%, Sigma - Aldrich Procedures: Testing protocols in accord with good laboratory practice were employed for all tests. The equipment and instrument calibrations verified current and within specification, prior to use. Materials for assessment were inventoried, numbered (if needed) and logged upon receipt. Fourteen filter cartridges were ev aluated for formaldehyde service life test. All the tests were performed in general accordance with NIOSH procedure TEB - APR - STP - 00 39A . Four cartridges, each, were subjected to low and high humidity conditioning, prior to service life test. Three sets of cartridges in the “As Received” state (AR) along with the humidity conditioned cartridges were then tested for formaldehyde service life as presented in the tables in the following page s . Both, the models model 242 and model 243 were used in pairs for eac h test.

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