Primary Device ID | 05404016610331 |
NIH Device Record Key | 8753bff5-6f06-471a-936c-ac3d5323750e |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Handi-Move Spreaderbar |
Version Model Number | 2120 00000002 |
Company DUNS | 283658730 |
Company Name | Handi-Move |
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 | false |
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 |