南非醫(yī)用口罩SAHPRA認(rèn)證

根據(jù)南非國(guó)家法律規(guī)定，醫(yī)療器械產(chǎn)品出口到南非必須要經(jīng)過(guò)南非國(guó)家健康藥品管理局注冊(cè)認(rèn)證，且要同時(shí)獲得Sales Permit方可在南非市場(chǎng)銷(xiāo)售。

在南非醫(yī)療器械法規(guī)中，按照風(fēng)險(xiǎn)等級(jí)將醫(yī)療器械分為以下四類(lèi)：

? Class A - Low Risk

? Class B - Low-moderate Risk

? Class C - Moderate-highRisk

? Class D - HighRisk

其中，醫(yī)用口罩適用標(biāo)準(zhǔn)是SANS1866-1/2，劃分為Class A。一般情況下，MCC/SAHPRA認(rèn)證都是直接簽發(fā)給你南非經(jīng)銷(xiāo)商或者南非代理。

西測(cè)國(guó)際認(rèn)證檢測(cè)中心在南非設(shè)有分公司，可以為中國(guó)口罩企業(yè)申請(qǐng)南非認(rèn)證提供當(dāng)?shù)卮砣朔?wù)（Authorized Representative）。以下是Authorized Representative的要求：

“authorised representative” means any natural person, resident in the Republic of South Africa, who

a) has the written mandate to represent a manufacturer, importer, distributor, wholesaler, retailer or service provider in the Republic;

b) acts on behalf of a manufacturer, importer, distributor, wholesaler, retailer or service provider for specified tasks with regard to the latter’s obligations and in whose name the manufacturer licence, distributor licence, wholesaler licence and or certificate of registration is issued; and

c) is responsible for all aspects of the medical device or IVD, including performance, quality, safety and compliance with conditions of registration, clinical trials or clinical investigations;

MCC/SAHPRA認(rèn)證主要需要以下資料：

? Full Name of legal person

? Company Registration Number or Individual Person’s IdentityNumber

? Physical address

? Postal address

? Telephone Number

? Nature of business activities: manufacture; importation; distribution; wholesaler or exportation

? Authorised Representative’s Name

? Authorised Representative’s work telephone number and mobile telephone number

? Authorised Representative’s email address