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  • FSC

    Certificate No : SA-COC-013140

    Issuing authority : Soil Association Certification LimitedSpear House

    Valid period : 2024/5/21 - 2029/5/20

    "the certified site" has been certified in accordance with therequirements of the Forest Stewardship Counci A.C. using the FSC®Chain of Custody standards* and that Goodwood Medical Care Ltd. of

    1-2 Floor, 3-919, Jiulicun, Yongzheng Street,, JinzhouDistrict, Dalian, Liaoning, 116100, CHINA

    is hereby licensed to use the FSC Logo on and sell as FSC certified allproducts listed on the attached FSC product schedule as FSC  

    Controlled Wood;FSC 100%.

    FSC Controlled Wood may be sold for the purposes of furthermixing.














  • SX

    Certificate No : 326009117-200

    Issuing authority : TÜV Rheinland LGA Products GmbH

    Valid period : 2024/7/12 - 2027/7/11

    Certificate
    Quality Management System
    EN ISO 13485:2016
    Registration No.:           SX 2174537-1
    Certificate Holder:         Goodwood Medical Care Ltd.
                                          3-919, Jiulicun, Yongzheng Street, Jinzhou District,
                                          Dalian,
                                          116100 Liaoning
                                           P.R. China
    Scope:                     
    Design and Development, Manufacture and Distribution of
    Sterile Tongue Depressors, Sterile Cotton Tipped Applicators,
    Transport Swabs, Cervical Scrapers, Cytology Brushes,
    Non-sterile Tongue Depressors, Non-sterile Applicators,
    Disposable sampling Swabs, Non-sterile Transport Swabs,
    Non-sterile Disposable Sampling SwabsNon-sterile Cervical
    Scrapers, Dry Scrub Brushes, Non-sterile Sponge Swabs,
    Dental Brushes, Wooden Sticks, Non-sterile Vaginal
    Speculums, Non-sterile Cytology Brushes

  • EU Certificate

    Certificate No : 244384642-200

    Issuing authority : CMC Medical Devices&Drugs S.L.

    Valid period : 2023/1/6 - 2027/11/3

    The Notified Body hereby declares that the reguirements of Annex X!, Part A of the REGULATION (EU)2017/745 have been met for the listed products. The above named manufacturer has established andapplies a production quality assurance, which is subject to periodic surveillance, defined by Annex Xl.Part A, Section 7 of the aforementioned regulation. lf class ll devices or class llb devices are coveredby this certificate, an EU type-examination certificate in accordance with Annex X of the aforementionedregulation is required before placing them on the market.