Primary Device ID | 17540262100013 |
NIH Device Record Key | 4b7a948b-6f82-4c42-84db-8df46635f3cb |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Change Healthcare Cardiology Hemo |
Version Model Number | 14.1 |
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 |