| Primary Device ID | 15019517088632 |
| NIH Device Record Key | abc9f756-eb9c-4e81-b148-cc18ce4b6d17 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | PharmGuard |
| Version Model Number | 22-4095-0204-25 |
| 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 | false |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 15019517088632 [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 | 2019-04-05 |
| 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 |