Primary Device ID | 00810051632378 |
NIH Device Record Key | ffb8601c-a0db-4116-867d-a740eea6ff1b |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | ICON 2 |
Version Model Number | 1539116500-1 |
Catalog Number | 1539116500 |
Company DUNS | 119290896 |
Company Name | Control Devices, LLC |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
MRI Safety Status | MR Conditional |
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 | true |
OTC Over-The-Counter | false |