Primary Device ID | 00190790001308 |
NIH Device Record Key | 1f484cd9-8a00-499d-b3de-3dd1e178d0c2 |
Commercial Distribution Discontinuation | 2018-12-31 |
Commercial Distribution Status | Not in Commercial Distribution |
Brand Name | iN∫X ® |
Version Model Number | 0015808 |
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 |