№ lp_1_26154
This document provides a checklist for manufacturers to ensure compliance with essential safety and performance principles for medical devices, including in-vitro diagnostic devices (IVDDs), across various design, manufacturing, and risk management aspects.
Year: 2022
Note: Region / city
Topic: Medical Devices, Safety, Compliance
Document Type: Checklist
Organization / institution: DFAR Department
Target Audience: Manufacturers, Regulatory Bodies, Medical Device Industry
Effective Date: 31/10/2022
Review Due Date: 30/10/2025
Price: 8 / 10 USD
The file will be delivered to the email address provided at checkout within 12 hours.

Don’t have cryptocurrency yet?

You can still complete your purchase in a few minutes:
  1. Buy Crypto in a trusted app (Coinbase, Kraken, Cash App or any similar service).
  2. In the app, tap Send.
  3. Select network, paste our wallet address.
  4. Send the exact amount shown above.
After sending, paste your TXID (transaction ID) and your email to receive the download link. Need help? Contact support and we’ll guide you step by step.