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CE_761168_Corpro_HM1500_F1200-(NB2797)-V1

CE_761168_Corpro_HM1500_F1200-(NB2797)-V1

CE_761168_Corpro_HM1500_F1200-(NB2797)-V1

Product catalog summary
Certificate Overview: This document is an EU Type Examination Certificate issued to The Filter Design Company Limited for a respiratory protective device. The certificate number is CE 761168, and it certifies compliance with Regulation (EU) 2016/425 concerning Personal Protective Equipment (PPE).
Product Specifications: The certified product is a respiratory protective device consisting of a half mask (Model: HM1500 Medi Half Mask) and a particle filter (Model: F1200 Filter). The device complies with EN 140:1998 for half masks and EN 143:2021 for particle filters. It is available in small, medium, and large sizes and features two bayonet-type ports for inhalation and exhalation filters.
Technical Specifications: The half mask is classified under EN 140, and the particle filter is classified as P3 R (re-usable) under EN 143. An independently certified visor is available as an optional accessory. The exhalation filter (Model F1200) meets the P2 R classification requirements of EN 143:2021.
Certificate Administration: The certificate was first issued on September 26, 2022, and is valid until September 26, 2027. The certificate's validity depends on maintaining conformity to type based on quality assurance of the production process, as referenced in BSI Certificate CE 678319.
Additional Information: The certificate is issued by BSI Group The Netherlands B.V., and any changes in the manufacturing process must be communicated to the Notified Body to maintain certificate validity. The certificate can be authenticated online or by contacting BSI Group The Netherlands.
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Catalog excerpts

CE_761168_Corpro_HM1500_F1200-(NB2797)-V1-1

bsi. EU Type Examination Certificate This is to certify that: Holds Certificate Number: The Filter Design Company Limited la Millfield Lane Haydock St Helens Merseyside WA119TW United Kingdom Respiratory protective device comprising of: Half mask to EN 140:1998 and a particle filter to EN 143:2021 Model: HM1500 Medi Half Mask and F1200 Filter. on the basis that BSI carried out the relevant Type Examination procedures under the requirements with the Regulation (EU) 2016/425 of the European Parliament and Council relating to Personal Protective Equipment Regulation (PPE) Annex V (Module B) and meets the relevant health and safety requirements specified in Annex II For and on behalf of BSI, a Notified Body for the above Regulation (Notified Body Number 2797): Drs. Dave Hagenaars, Managing Director Expiry Date: 2027-09-26 Page: 1 of 3 This certificate has been issued by and remains the property of BSI Group The Netherlands B.V., John M. Keynesplein 9, 1066 EP Amsterdam, The Netherlands and should be returned immediately upon request. ·,o check its validity telephone +31 20 3460780. An electronic certificate can be authenticated online. BSI Group The Netherlands B.V., registered in the Netherlands under number 33264284, at John M. Keynesplein 9, 1066 EP Amsterdam, The Netherlands A member of BSI Grouo of Companies.

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CE_761168_Corpro_HM1500_F1200-(NB2797)-V1-2

Page: 2 of 3 This certificate has been issued by and remains the property of BSI Group The Netherlands B.V., John M. Keynesplein 9, 1066 EP Amsterdam, The Netherlands and should be returned immediately upon request. To check its validity telephone +31 20 3460780. An electronic certificate can be authenticated online. BSI Group The Netherlands B.V., registered in the Netherlands under number 33264284, at John M. Keynesplein 9, 1066 EP Amsterdam, The Netherlands A member of BSI Group of Companies.

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CE_761168_Corpro_HM1500_F1200-(NB2797)-V1-3

EU Type Examination Certificate No. CE 761168 Certificate Administration Details Technical File Reference: HM1500 and F1200 Technical File, HM1500 & F1200 Medi Range. Certificate Administration Record Comments First issue. Certificate validity Issue date The Certificate holder is responsible for keeping the Notified Body advised of changes to any aspect of the overall process used in the manufacture of the products, failure to do so could invalidate the Certificate in respect of product manufactured following the introduction of such changes. Monitoring of manufactured PPE The validity of the...

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