Primary Device ID | 00190790001322 |
NIH Device Record Key | 93f1dfab-db65-4adc-81c0-aeaacf96f7df |
Commercial Distribution Discontinuation | 2018-12-31 |
Commercial Distribution Status | Not in Commercial Distribution |
Brand Name | iN∫X ® |
Version Model Number | 0015810 |
Company DUNS | 004239034 |
Company Name | FERNO-WASHINGTON, 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 |
00190790001612 | iN∫X ® for iN∫Line™, Integrated Patient Transport & Loading System – conversion |
00190790001353 | iN∫X ® for iN∫Line™, Integrated Patient Transport & Loading System – DWL,SX |
00190790001346 | iN∫X ® for iN∫Line™, Integrated Patient Transport & Loading System – SX |
00190790001339 | iN∫X ® for iN∫Line™, Integrated Patient Transport & Loading System – DWL |
00190790001322 | iN∫X ® for 175, Integrated Patient Transport & Loading System – DWL,SX |
00190790001315 | iN∫X ® for 175, Integrated Patient Transport & Loading System – SX |
00190790001308 | iN∫X ® for 175, Integrated Patient Transport & Loading System – DWL |