| Primary Device ID | 15019517177381 | 
| NIH Device Record Key | f455fd63-9406-4785-b5b4-7c19a930313f | 
| Commercial Distribution Status | In Commercial Distribution | 
| Brand Name | PharmGuard | 
| Version Model Number | 22-0004-0205-25 | 
| 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 | 15019517177381 [Primary] | 
| FRN | Pump, infusion | 
| Steralize Prior To Use | false | 
| Device Is Sterile | false | 
| Public Version Status | New | 
| Device Record Status | Published | 
| Public Version Number | 1 | 
| Public Version Date | 2020-03-30 | 
| Device Publish Date | 2020-03-20 | 
| 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 |