Surgical masks · certification

Surgical Mask Certification Guide

CE marking, FDA registration and ISO 13485 — what these mean for exporting surgical masks and which files to verify.

Руководство покупателя

Что учесть

01

CE marking under the EU Medical Device Regulation

Medical face masks sold in Europe must carry CE marking under the EU Medical Device Regulation (MDR) or the applicable harmonised standard. The CE file confirms the mask meets the required safety and performance requirements, and it must name the exact model you are ordering. A certificate that covers a similar but different model is not proof your order is compliant, so check the model reference, the issuing body and the validity period before you commit.

  • CE marking is required for medical face masks in Europe
  • The file must name the exact model you order
  • Check the issuing body, standard and validity period
02

FDA registration for the US market

Surgical masks sold in the US are regulated as medical devices by the FDA. Confirm the supplier's FDA registration and that the specific model is covered before ordering for the US market. Registration is establishment-level, so verify the facility and the product listing match the mask you intend to import, and keep the documentation for your own customs and market-entry file.

03

ISO 13485 quality management

ISO 13485 is the quality management standard for medical device manufacturers. A supplier with ISO 13485 certification demonstrates a controlled production process covering design, manufacturing and quality control, which supports consistent product quality across batches. For institutional buyers, an ISO 13485-certified supplier is often a baseline requirement before a contract is considered.

04

What to request from your supplier

Ask for the certification file covering the exact model, the standard it meets, the issuing body and the validity period. Verify the file is current and matches your target market before placing an order, and keep a copy on file for your own market entry. If you plan to sell under your own brand, confirm whether the certification can be issued under your brand or remains under the manufacturer's name.

  • Exact model reference on the certificate
  • Standard, issuing body and validity period
  • Certification under your brand or the manufacturer's
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Перейдите для просмотра полных спецификаций и сертификационных файлов.

Surgical Mask 3-Ply Blue – EN 14683 Type II 3-ply meltblown surgical mask for clinical use
CE / FDA

Хирургическая маска 3-слойная синяя

EN 14683 Type II хирургическая маска с трехслойной конструкцией из мелтблауна. Стандартный барьер для инфекционного контроля для больниц, клиник и общего медицинского применения.

Сертификационный файлView
Surgical Mask Type IIR White surgical mask
CE / FDA

Хирургическая маска Type IIR белая

Белая хирургическая маска типа IIR с петлями за уши для стоматологии, дерматологии и пищевой промышленности. Сертифицирована по EN 14683, эффективность бактериальной фильтрации ≥98%, устойчивость к брызгам 120 мм рт. ст. Трёхслойная конструкция с мелтблаун-фильтром, 50 шт. в коробке. Маркировка CE, производство Justsun.

Сертификационный файлView
Surgical Mask Anti-Fog Blue – blue surgical mask with anti-fog PE strip, EN 14683 Type IIR, ≥98% BFE
CE / FDA

Хирургическая маска антизапотевающая, синяя

Синяя хирургическая маска с антизапотевающей полосой из ПЭ-пленки. EN 14683 Тип IIR, ≥98% BFE, устойчивость к брызгам 120 мм рт. ст. Предотвращает запотевание очков у хирургов, стоматологов и лабораторного персонала. 50 шт. в коробке.

Сертификационный файлView
Часто задаваемые вопросы покупателей

Частые вопросы о покупке

Is CE marking required for all surgical masks in Europe?+

Yes, medical face masks sold in Europe must carry CE marking under the applicable regulation. Confirm the file covers the exact model you are ordering.

What is the difference between CE and FDA?+

CE marking is required for the European market, while FDA registration is required for the US. They are separate approvals under different regulatory systems.

Why does ISO 13485 matter?+

ISO 13485 certifies a quality management system for medical device manufacturing. It supports consistent production quality and is often expected by institutional buyers.

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  • Сертификационные файлы CE / FDA
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