Primary Device ID | 07290018016152 |
NIH Device Record Key | b402536f-c2c5-429e-b26e-092187017305 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | HealthFLD |
Version Model Number | 1.0 |
Company DUNS | 600098228 |
Company Name | NANO-X AI LTD |
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 | false |
Serial Number | false |
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 | 07290018016152 [Primary] |
JAK | System, X-Ray, Tomography, Computed |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-11-29 |
Device Publish Date | 2024-11-21 |
07290018016176 - HealthCCSng | 2025-02-27 - |
07290018016152 - HealthFLD | 2024-11-29 |
07290018016152 - HealthFLD | 2024-11-29 |
07290018016169 - HealthCCSng | 2024-11-29 |
07290018016145 - HealthOST | 2023-05-17 |
07290018016138 - HealthCCSng | 2023-05-12 |
07290018016114 - HealthOST | 2022-08-09 |
07290018016077 - HealthPNX | 2022-03-28 |