| Primary Device ID | 00840155408197 |
| NIH Device Record Key | 0ebff32b-96e6-4f1c-97ba-6a8e72c421e2 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | MedSource Extrication Device |
| Version Model Number | MS-ED3000 |
| Catalog Number | Not Applicable |
| Company DUNS | 041674552 |
| Company Name | MEDSOURCE INTERNATIONAL 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 | false |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | false |
| 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 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00840155408173 [Primary] |
| GS1 | 00840155408197 [Package] Contains: 00840155408173 Package: Case [4 Units] In Commercial Distribution |
| CCX | Support, Patient Position |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2021-08-09 |
| Device Publish Date | 2021-07-30 |
| 00816703025925 | Extrication Device |
| 00840155408197 | Extrication Device, Red |
| 00840155408166 | Extrication Device, Pediatric |
| 00840155404014 | Extrication Device ONLY, No Bag |
| 00840155410589 | Extrication Device |
| 00840155410565 | Extrication Device, Bomberos |
| 00840155410558 | Extrication Device, Green |
| 00840155408142 | Extrication Device, MedStorm |