Primary Device ID | 00817770020622 |
NIH Device Record Key | a07880da-c539-49a2-ab16-d7eb237e289b |
Commercial Distribution Discontinuation | 2019-05-06 |
Commercial Distribution Status | Not in Commercial Distribution |
Brand Name | PULSOX-300 |
Version Model Number | R204P16-002 |
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 | 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 | false |
OTC Over-The-Counter | false |