| Primary Device ID | 10884450303914 | 
| NIH Device Record Key | dffa2ac0-8b9c-441b-bd86-f24def30f23f | 
| Commercial Distribution Status | In Commercial Distribution | 
| Brand Name | Advocate™ | 
| Version Model Number | 00884450303917 | 
| Catalog Number | A18050200150/A | 
| Company DUNS | 184763290 | 
| Company Name | Merit Medical Systems, 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 | 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 | false | 
| RX Perscription | false | 
| OTC Over-The-Counter | false | 
| Device Issuing Agency | Device ID | 
|---|---|
| GS1 | 00884450303917 [Primary] | 
| GS1 | 10884450303914 [Package] Contains: 00884450303917 Package: [10 Units] In Commercial Distribution | 
| LIT | Catheter, angioplasty, peripheral, transluminal | 
| Steralize Prior To Use | false | 
| Device Is Sterile | false | 
| Public Version Status | Update | 
| Device Record Status | Published | 
| Public Version Number | 2 | 
| Public Version Date | 2019-08-09 | 
| Device Publish Date | 2019-07-26 | 
| 10884450300883 | 00884450300886 | 
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