Nzira yekutarisa chokwadi chemasikisi ekurapa

OIP-Cth
Sezvo masiki ekurapa akanyoreswa kana kudzorwa zvinoenderana nemidziyo yekurapa munyika zhinji kana matunhu, vatengi vanogona kuwedzera kuasiyanisa kuburikidza nekunyoresa kwakakodzera uye kutonga ruzivo.Unotevera muenzaniso weChina, United States neEurope.

China
Masks ekurapa ndeekirasi yechipiri yemidziyo yekurapa muChina, iyo yakanyoreswa uye inotungamirwa nedhipatimendi redunhu redhipatimendi, uye inogona kubvunzwa nemidziyo yekurapa kubvunza nhamba yekuwana mudziyo wekurapa.Link ndeiyi:

http://www.nmpa.gov.cn/WS04/CL2590/.

Nyika dzakabatana
Zvigadzirwa zveMask izvo zvakatenderwa neUS FDA zvinogona kubvunzwa kuburikidza neyayo yepamutemo webhusaiti kutarisa nhamba yechitupa chekunyoresa, chinongedzo ndechekuti:

https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfPMN/pmn.cfm

Pamusoro pezvo, zvinoenderana nePOLICY yazvino yeFDA, parizvino inozivikanwa seMask yeChinese Standards pasi pemamwe mamiriro, uye chinongedzo chemabhizinesi ayo ane mvumo ndeichi:

https://www.fda.gov/media/136663/download.

European Union
Kutengeswa kunze kweEU masks ekurapa anogona kuitwa kuburikidza neakatenderwa Matumbi Akaziviswa, ayo Body Yakaziviswa yakabvumidzwa neEU Medical Device Directive 93/42/EEC (MDD) iri:

https://ec.europa.eu/growth/tools-databases/nando/index.cfm?fuseaction=directive.notifiedbody&dir_id=13.

Kero yakaziviswa yedare rekubvunza yakabvumidzwa neEU Medical Device Regulation EU 2017/745 (MDR) ndeiyi:

https://ec.europa.eu/growth/tools-databases/nando/index.cfm?fuseaction=directive.notifiedbody&dir_id=34.


Nguva yekutumira: Kubvumbi-17-2022