Page 14 - CATALOGO MASCARILLAS QUIRÚRGICAS TIPO IIR

Page 5 of 12 Report No. 60377885 001

Testing

Date of receipt of test item(s) ............................. : See cover page
Dates of tests performed................................... : See cover page

Possible test case verdicts:
- test case does not apply to the test object ............. : N/A
- test object does meet the requirement .................. : P (Pass)
- test object was not evaluated for the requirement ... : N/E (collateral standards only)
- test object does not meet the requirement ............. : F (Fail)

General remarks:
"(See Attachment #)" refers to additional information appended to the report.
"(See appended table)" refers to a table appended to the report.
The tests results presented in this report relate only to the object tested.
This report shall not be reproduced except in full without the written approval of the testing laboratory.
List of test equipment must be kept on file and available for review.
Additional test data and/or information provided in the attachments to this report.

Throughout this report a comma / point is used as the decimal separator.

Name and address of factory (ies) ......................: Same as the applicant

General product information:
1, The tested medical mask classified as type IIR.
2, The Biocompatibility (clause 5.2.6) is not evaluated in this test report.
3, The test results are for reference only. Relevant certification may be needed if the mask is
intended to be sold in Europe.

QMF-RT-33008SHG Revision number: 1.0 Effective date: 2020-03-12