Primary Device ID | 00852753008907 |
NIH Device Record Key | 589a387a-c84b-4f86-9377-170ebaa5cb0b |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Decompression of Choice |
Version Model Number | E9011 |
Company DUNS | 826316098 |
Company Name | PIVOTAL HEALTH SOLUTIONS, INC. |
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 | true |
OTC Over-The-Counter | false |