Primary Device ID | 00810045921860 |
NIH Device Record Key | 159a9f08-b4b5-4ecb-a576-a387e0889b23 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Alumi-Hand PLUS |
Version Model Number | KH-860-Single |
Catalog Number | KH-860-Single |
Company DUNS | 041517095 |
Company Name | INSTRUMENT SPECIALISTS, 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 | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | true |
RX Perscription | true |
OTC Over-The-Counter | false |