Primary Device ID | 15019517225471 |
NIH Device Record Key | 4643e2e1-af2e-457a-bd82-14ecaf22bc30 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | PharmGuard |
Version Model Number | 22-0004-0206-25 |
Company DUNS | 082005361 |
Company Name | Smiths Medical ASD, 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 | 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 | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 15019517225471 [Primary] |
PHC | Infusion safety management software |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2021-11-24 |
Device Publish Date | 2021-11-16 |
15019517157888 | 22-0117-0201-25 |
15019517157871 | 22-0004-0204-25 |
15019517088632 | 22-4095-0204-25 |
15019517151107 | 22-4075-0301-51 |
15019517197112 | 21-2194-0403-25 |
15019517177381 | 22-0004-0205-25 |
15019517177374 | 22-0117-0202-25 |
15019517177367 | 22-4095-0205-25 |
15019517225495 | 22-4095-0206-25 |
15019517225488 | 22-0117-0203-25 |
15019517225471 | 22-0004-0206-25 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() PHARMGUARD 78728803 not registered Dead/Abandoned |
Biomedical Equipment & Engineering Services Co Inc. 2005-10-07 |
![]() PHARMGUARD 76578584 3055986 Live/Registered |
SMITHS MEDICAL ASD, INC. 2004-03-02 |