---
title: Polish Medical Device Registration Form Template with CE Marking Verification | Paperform
description: Complete Polish medical device registration form template with CE marking verification, notified body details, NIP/REGON/KRS fields, and health ministry compliance for medical device manufacturers and distributors.
url: "https://paperform.co/templates/polish-medical-device-registration-form"
type: static
generatedAt: "2026-03-28T00:44:50.920Z"
---

[← Back to free form templates](/templates/)    ![Polish Medical Device Registration Form](https://img.paperform.co/fetch/f_webp/https://d3gw2uv1ch7vdq.cloudfront.net/content/form_templates/assets/polish-medical-device-registration-form.png)
    [Preview](https://_preview.paperform.co/ai-template/polish-medical-device-registration-form) [Use this template for free](/create?ai-template=polish-medical-device-registration-form)    [Legal & Compliance Forms](/templates/category/legal/)[Industry-Specific Forms](/templates/category/industry-specific/) [Healthcare](/templates/industry/healthcare/) [Manager](/templates/role/manager/)[Healthcare Administrator](/templates/role/healthcare-admin/)[Compliance Officer](/templates/role/compliance-officer/)     About this free form template
Medical device manufacturers and distributors need to navigate complex Polish regulatory requirements when registering devices for the Polish market. This **Polish Medical Device Registration Form** streamlines the entire process, capturing all mandatory information required by the Polish Ministry of Health and ensuring compliance with both EU Medical Device Regulations and Polish-specific requirements.

Built for medical device manufacturers, importers, authorized representatives, and regulatory affairs professionals, this template collects essential company identification data (NIP, REGON, KRS), CE marking verification, notified body certification details, device classification, and comprehensive technical documentation in one structured workflow. The form handles everything from Class I devices through high-risk Class III implantable devices, adapting the required fields based on your specific device classification.

**Paperform** makes regulatory compliance faster and more accurate by replacing scattered PDF documents and email chains with a single, professional form that collects structured data, validates Polish tax and registration numbers, and creates a complete audit trail of your submission. The conditional logic ensures you only see fields relevant to your device class, reducing confusion and submission errors.

Once submitted, integrate with **Stepper** to automate your registration workflow—automatically route submissions to different team members based on device class, trigger follow-up tasks for missing documentation, send notifications to regulatory affairs teams, and maintain synchronized records across your document management systems and CRMs. This automation ensures nothing falls through the cracks during the critical registration process.

Whether you're a multinational medical device company entering the Polish market or a local distributor managing multiple product registrations, this template provides the professional foundation you need for regulatory compliance while maintaining the flexibility to adapt to Poland's evolving medical device regulations.
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