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Ihe mkpuchi ihu ịwa ahụ (F-Y1-A Ụdị IIR)

Ụdị: F-Y1-A Ụdị IIR
Ụdị: Ụdị dị larịị
Ụdị eyi: Nkwado ntị
Valve: Ọ dịghị
Ọkwa nzacha: BFE98, Ụdị IIR
Agba: Blue
Ọkọlọtọ onye isi: EN14683-2019+AC:2019
Nkọwa nkwakọ ngwaahịa: 10pcs/bag, 3000pcs/CTN


Nkọwa ngwaahịa

Ozi

OZI MGBAKWUNYE

Ihe mejupụtara
A na-emepụta usoro nzacha na oyi akwa site na elu 25g na-abụghị nke a kpara akpa, oyi akwa nke abụọ 25g BFE99 filtration, oyi akwa dị n'ime 25g anaghị kpara akpa.

Oke ngwa
A na-eji ya kpuchie ọnụ, imi na agba nke onye ọrụ, ma na-enye ihe mgbochi anụ ahụ iji gbochie nnyefe kpọmkwem nke microorganisms pathogenic, mmiri ara, ihe ndị ọzọ, wdg.

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  • Nke gara aga:
  • Osote:

  • F-Y1-A bụ ihe mkpuchi ihu ịwa ahụ.
    Koodu UMDN: 12-458
    Nhazi: Klas 1
    Iwu: Dịka Iwu 1 siri dị, Mgbakwunye V111, Isi nke Atọ nke (EU) MDR 2017/745
    Ụzọ ntule ndakọrịta: ANNEX II + ANNEX III + Nkeji edemede 19 nke (EU) MDR 2017/745

    Ọ bụ onye nrụpụta kwupụtara na F-Y1-A na-ezute inye iwu nke Medical Device Regulation (EU) MDR 2017/745 nke European Parliament na Council of 5 April 2017 na ngwaọrụ ahụike.A na-eji nkwekọrịta nkwupụta EU n'okpuru ọrụ naanị nke onye nrụpụta.

    Ọkọlọtọ F-Y1-A etinyere:
    EN ISO 13485: 2016, EN ISO 14971: 2012, EN 14683: 2019 +AC: 2019, BS EN ISO 15223-1: 2016, EN ISO 10933-1: 2009 / AC: 2010: 90-5 ISO 10993-10:2010, EN 1041:2008