Primary Device ID | 10851607003126 |
NIH Device Record Key | a4d3d3b2-e88e-494d-9f3f-1765010e62f8 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Monitor System, Patient Display |
Version Model Number | 43T2564 |
Company DUNS | 962187964 |
Company Name | MEDSPIRA, LLC |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
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 | true |
Manufacturing Date | false |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | false |
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