Primary Device ID | 00817081026542 |
NIH Device Record Key | fb83b3a0-d9c9-4f82-8acd-a658a2d7e9af |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Syringe, Calibration, 3 Liter, Aluminum, SDI Diagnostics |
Version Model Number | Syringe, Calibration, 3 Liter, Aluminum, SDI Diagn |
Catalog Number | 192719 |
Company DUNS | 020275145 |
Company Name | A-M SYSTEMS, 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 | true |
Serial Number | true |
Manufacturing Date | true |
Expiration Date | true |
Donation Id Number | true |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
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