Primary Device ID | 00817698020681 |
NIH Device Record Key | 3d11d7f5-6342-4814-8539-44ddd2c74de0 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Healthcare Logiix Systems |
Version Model Number | Dream |
Company DUNS | 079452927 |
Company Name | HEALTHCARE LOGISTICS SYSTEMS LLC |
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 | 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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00817698020681 [Primary] |
DQA | Oximeter |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-05-09 |
Device Publish Date | 2024-05-01 |
00817698020681 - Healthcare Logiix Systems | 2024-05-09 |
00817698020681 - Healthcare Logiix Systems | 2024-05-09 |
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