SRS-083 Display the legal information about this medical device
Identifier​
SRS-083
Software System​
- API
- Backend
Category​
- Regulatory
Description​
The device shall display the legal information about this medical device according to FDA and MDR regulations:
- Intended purpose
- Warning indicating that the user manual must be read and use the device as described
- UDI: The Unique Device Identifier
- Quantity:
- Manufacturer information: the company name and address.
- Date of manufacture: date of the software release.
- Contact info
- Country of manufacture:
- CE:
- CE certification body: 2797.
- User manual: symbol followed the clickable link to the user manual
- MD: Symbol that indicates that this software is a medical device.
- Version
Derived from PRS​
PRS-3YH
: Compliance with MDRPRS-6DP
: Compliance with FDA