Primary Device ID | 17540262090024 |
NIH Device Record Key | b3e4484c-a7f7-4604-82c0-6b7b25a10972 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Change Healthcare Cardiology |
Version Model Number | 14.1.1 |
Company DUNS | 600748180 |
Company Name | CHANGE HEALTHCARE ISRAEL LTD |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | MR Unsafe |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | false |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
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 |