Primary Device ID | 00860012325092 |
NIH Device Record Key | 7b0eb61f-46aa-484f-a72b-1c58a550df2e |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Phoenix Thera-Lase system |
Version Model Number | 70W |
Company DUNS | 079869313 |
Company Name | PHOENIX THERA-LASE SYSTEMS, 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 | true |
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 |