Primary Device ID | 10887787009139 |
NIH Device Record Key | ac2de26a-d4eb-4950-bf20-e3ed97deb5b1 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | ICU Medical MedNet |
Version Model Number | 6.31.01 |
Catalog Number | 160379202 |
Company DUNS | 118380146 |
Company Name | ICU MEDICAL, INC. |
Device Count | 1 |
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 | false |
Lot Batch | false |
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 |
Phone | +1(800)241-4002 |
TSC.Support@icumed.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 10887787009139 [Primary] |
PHC | Infusion safety management software |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2020-01-22 |
Device Publish Date | 2018-12-10 |
10887787009139 | Mednet Software |
10887709101811 | Mednet Software |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
ICU MEDICAL MEDNET 87356803 not registered Live/Pending |
ICU Medical, Inc. 2017-03-02 |