Primary Device ID | 00817369021238 |
NIH Device Record Key | 3e2a035d-3991-4649-ba99-381e0406ddcd |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Pulse Pro Lower Body Recovery Package |
Version Model Number | Pulse Pro Recovery Package - Lower Body Power Shor |
Catalog Number | 40223 |
Company DUNS | 111448069 |
Company Name | NORMATEC INDUSTRIES LP |
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 | 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 | true |