Primary Device ID | 00865309000287 |
NIH Device Record Key | e26ab333-0abf-4c72-bbbd-7edcd82bc1cc |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | DiLumen Ig Interventional Grasper |
Version Model Number | DiLumen Ig 95 cm |
Catalog Number | D-3000 |
Company DUNS | 859290897 |
Company Name | LUMENDI LLC |
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 | false |
RX Perscription | true |
OTC Over-The-Counter | false |