Primary Device ID | 00853061006500 |
NIH Device Record Key | 132fcd11-fa01-49a2-adb9-c68265c7253e |
Commercial Distribution Discontinuation | 2019-05-06 |
Commercial Distribution Status | Not in Commercial Distribution |
Brand Name | MAX-250E |
Version Model Number | R125P03-003 |
Company DUNS | 169911828 |
Company Name | MAXTEC, LLC |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
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 |