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Healthcare

Medical Device Documentation

Document medical device manufacturing, testing, and deployment with cryptographic proof. Verified evidence for FDA submissions, field safety notices, and post-market surveillance.

The Problem

FDA Submission Rejections

Device submissions rejected due to insufficient evidence of testing and manufacturing conditions.

Product Liability

Device failures lead to litigation. Manufacturers need verifiable proof of proper manufacturing and testing.

How Immutis Helps

Hardware-backed cryptographic proof integrated into your existing workflow.

Manufacturing Evidence

Document device manufacturing and testing with hardware-attested proof. FDA-submission ready.

Field Surveillance

Post-market device monitoring with verified evidence. Rapid response to safety issues.

Key Features

UDI Integration

Tie captures to unique device identifiers

FDA Ready

Documentation format meets submission requirements

Compliance

Meets industry standards and regulatory requirements

FDA 21 CFR Part 820ISO 13485MDRSOC 2

Ready to verify every capture?

Start your pilot program and see the difference cryptographic proof makes.

Start Device Pilot