Primary Device ID | 00817369021115 |
NIH Device Record Key | cc5c1bef-8d6c-4c8b-974d-c2f60b8c4f96 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Pulse Full Body Recovery Package |
Version Model Number | Pulse Recovery Package - Full Body Power Standard |
Catalog Number | 40144 |
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 |