Primary Device ID | 00850008449826 |
NIH Device Record Key | 96c10303-1f90-4752-b7bd-3298dd4e4a56 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Trademark Elevating Table |
Version Model Number | E9012-L |
Company DUNS | 826316098 |
Company Name | PIVOTAL HEALTH SOLUTIONS, INC. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
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 |