Primary Device ID | 00628011382177 |
NIH Device Record Key | 5b4d6192-e54f-4303-9586-dad5003bbcec |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Limbus Contour |
Version Model Number | 1.7.0 |
Company DUNS | 204682821 |
Company Name | Limbus Ai Inc. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | false |
Lot Batch | true |
Serial Number | true |
Manufacturing Date | true |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00628011382177 [Primary] |
LLZ | System, Image Processing, Radiological |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2023-04-24 |
Device Publish Date | 2023-04-14 |
00628011382146 | Limbus Contour is a stand-alone software medical device. It is a single purposes cross-platform |
00628011382153 | Limbus Contour is a stand-alone software medical device. It is a single purposes cross-platform |
00628011382160 | Limbus Contour is a stand-alone software medical device. It is a single purposes cross-platform |
00628011382177 | Limbus Contour is a stand-alone software medical device. It is a single purposes cross-platform |