Primary Device ID | 20357515085430 |
NIH Device Record Key | 05fc0b47-6a7c-4182-83cd-cf8934147fe3 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Health Wise |
Version Model Number | 580118 |
Company DUNS | 024723541 |
Company Name | ULTIMED, INC. |
Device Count | 100 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
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 | true |
RX Perscription | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00357515710031 [Unit of Use] |
GS1 | 20357515085430 [Primary] |
FMI | Needle, Hypodermic, Single Lumen |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2016-09-28 |
20357515085836 | 555649 |
20357515085638 | 555623 |
20357515085430 | 580118 |