Primary Device ID | 00860017001205 |
NIH Device Record Key | eda203be-f529-4d87-b4a3-f14221687411 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | GO IO |
Version Model Number | 1 |
Company DUNS | 098121274 |
Company Name | EINSTEIN WORKS, 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 | true |
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 | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00860017001205 [Primary] |
GS1 | 00860017001212 [Package] Package: case as each [12 Units] In Commercial Distribution |
OJA | Intravenous Extension Tubing Set |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2020-09-09 |
Device Publish Date | 2020-09-01 |
00860017001205 | Intraosseous Start Kit |
10850026832119 | Intraosseous Start Kit w/ Fixation |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() GO IO 79301511 not registered Live/Pending |
WAISMED LTD. 2020-09-09 |