| Primary Device ID | 20884450289321 | 
| NIH Device Record Key | 77c13e98-ce94-4dca-97e2-e5336a7ee7a1 | 
| Commercial Distribution Status | In Commercial Distribution | 
| Brand Name | Prelude EASE™ | 
| Version Model Number | 10884450289324 | 
| Catalog Number | PHR6F11025PW/C | 
| Company DUNS | 184763290 | 
| Company Name | Merit Medical Systems, Inc. | 
| Device Count | 5 | 
| DM Exempt | false | 
| Pre-market Exempt | false | 
| MRI Safety Status | Labeling does not contain MRI Safety Information | 
| Human Cell/Tissue Product | false | 
| Device Kit | true | 
| 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 Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
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| Device Size Text, specify | 0 | 
| Device Issuing Agency | Device ID | 
|---|---|
| GS1 | 00884450289327 [Unit of Use] | 
| GS1 | 10884450289324 [Primary] | 
| GS1 | 20884450289321 [Package] Contains: 10884450289324 Package: [4 Units] In Commercial Distribution | 
| DYB | INTRODUCER, CATHETER | 
| Steralize Prior To Use | false | 
| Device Is Sterile | true | 
| Public Version Status | Update | 
| Device Record Status | Published | 
| Public Version Number | 4 | 
| Public Version Date | 2021-10-11 | 
| Device Publish Date | 2017-02-08 | 
| 20884450257931 | 10884450257934 | 
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| 20884450289321 | 10884450289324 |