Zvigadzirwa zveSilicone nezvimwe zvinhu zvakafanana neyakasiyana certification, silicone zvigadzirwa certification report zvakateerana (ROHS, REACH, FDA, LFGB, UL, nezvimwewo).

 

JWT Rubberndeye yakagadzirirwa silicone chigadzirwa chinogona kupasa zvinotevera bvunzo uye zvitupa

1, RoHS

RoHS Chirevo ichi chakazvarwa muna Ndira 2003, European Parliament neEuropean Council vakapa rairo pamusoro pekurambidzwa kwekushandiswa kwezvimwe zvinhu zvine njodzi mumagetsi nemagetsi midziyo (Directive 2002/95/EC), inova kekutanga kuti RoHS. akasangana nenyika.Muna 2005, European Union yakaita wedzero kuna 2002/95/EC nenzira yechisarudzo 2005/618/EC, ichidudza miganhu yezvinhu zvitanhatu zvine njodzi.

Chirevo cheROHS ishumo yezvakatipoteredza.European Union yakatanga kushandisa RoHS zviri pamutemo musi waChikunguru 1, 2006.

2, SVIKA

Kusiyana neRoHS Directive, REACH inovhara nzvimbo yakakura.Ikozvino yawedzera kusvika 168 bvunzo, ndiyo European Union yakagadzwa, uye yakaitwa muna Chikumi 1, 2007 kemikari regulatory system.

Asi izvo zvinokanganisa kubva kumigodhi kusvika kune inenge yese indasitiri senge machira, indasitiri yemwenje, michina uye zvigadzirwa zvemagetsi uye maitiro ekugadzira, uku kugadzirwa kwemakemikari, kutengeserana, kushandisa kuchengetedzwa kwezvirongwa zvemitemo, mitemo yakagadzirirwa kuchengetedza hutano hwevanhu uye kuchengetedzwa kwezvakatipoteredza, kuchengetedza nekusimudzira kukwikwidzana kweindasitiri yemakemikari yeEuropean, uye kuvandudza kugona kweasina chepfu asingakuvadzi makomisheni, kudzivirira kupatsanurwa kwemusika, Kuwedzera kujeka kwekushandiswa kwemakemikari, kukurudzira kusiri kwemhuka kuyedzwa, uye kutsvaga budiriro yemagariro.REACH inogadza pfungwa yekuti nzanga haifanirwe kuunza zvitsva zvekushandisa, zvigadzirwa kana matekinoroji kana kukuvadza kwazvinogona kusingazivikanwe.

3, FDA

FDA: ndeimwe yemasangano ekusimbisa akagadzwa nehurumende yeUS mukati meDhipatimendi reHutano neHuman Services (DHHS) uye dhipatimendi rePublic Health (PHS).Sesangano rinotonga sainzi, iyo FDA inopihwa mhosva yekuona kuchengetedzeka kwechikafu, zvekuzora, zvinodhaka, biologics, michina yekurapa uye zvigadzirwa zveradiological zvinogadzirwa kana kuendeswa kuUnited States.Yaive imwe yekutanga masangano emubatanidzwa kuve nekuchengetedzwa kwevatengi sebasa rayo rekutanga.Inobata hupenyu hwemugari wese weAmerica.Pasi rose, FDA inozivikanwa seimwe yepasirese masangano anodzora chikafu nemishonga.Dzimwe nyika zhinji dzinotsvaga uye kugashira rubatsiro rweFDA kusimudzira nekutarisa kuchengetedzwa kwezvigadzirwa zvavo.Mutariri weChikafu neDrug Administration (FDA): Kutarisisa uye kuongororwa kwechikafu, zvinodhaka (kusanganisira mishonga yemhuka), zvishandiso zvekurapa, zvekuwedzera zvekudya, zvekuzora, chikafu chemhuka nezvinodhaka, waini nezvinwiwa zvine doro risingasviki 7%, uye zvigadzirwa zvemagetsi;Kuedza, kuongorora uye kupihwa chitupa chemhedzisiro yeionic uye isiri-ionic mwaranzi pahutano hwevanhu nekuchengetedzeka kunobva mukushandiswa kana kushandiswa kwezvigadzirwa.Zvinoenderana nemirairo, zvigadzirwa izvi zvinofanirwa kuyedzwa neFDA kuti zvive zvakachengeteka zvisati zvatengeswa pamusika.Iyo FDA ine simba rekuongorora vanogadzira uye kupomera vanotyora.

4.LFGB

LFGB ndiyo inonyanya kukosha gwaro remutemo pakutonga kwehutsanana hwechikafu muGermany, uye ndiyo nhungamiro uye musimboti wemimwe mitemo yakakosha yehutsanana hwechikafu.Asi pane shanduko mumakore achangopfuura, kunyanya kuenderana neEuropean standard.Mitemo inoita zvakajairwa uye zvekutanga zviga pane zvese zvechikafu cheGerman, chikafu chese pamusika weGerman uye zvese zvinodikanwa zvezuva nezuva zvine chekuita nechikafu zvinofanirwa kuenderana nezvinodiwa zvemitemo.Zvinyorwa zvezuva nezuva zvinosangana nechikafu zvinogona kuyedzwa uye kusimbiswa se "zvigadzirwa zvisina kemikari uye zvine muchetura zvinhu" neLFGB test report yakapihwa nemasangano ane mvumo, uye inogona kutengeswa mumusika weGerman.