Primary Device ID | 00840155408142 |
NIH Device Record Key | d86510af-ef5e-49a0-acd6-cad2f940b9ac |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | MedSource Extrication Device |
Version Model Number | STORM-ED2253 |
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 | 00840155408142 [Package] Contains: 00840155408159 Package: Case [4 Units] In Commercial Distribution |
GS1 | 00840155408159 [Primary] |
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 | 2021-09-02 |
Device Publish Date | 2021-08-25 |
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 |