| Primary Device ID | 00816777025999 | 
| NIH Device Record Key | 6d584cdf-e001-419b-9ef8-697e57d60d00 | 
| Commercial Distribution Status | In Commercial Distribution | 
| Brand Name | LVIS | 
| Version Model Number | 212917-LVIS-D-HDE | 
| Catalog Number | 212917-LVIS | 
| Company DUNS | 003263105 | 
| Company Name | MICROVENTION INC. | 
| Device Count | 1 | 
| DM Exempt | true | 
| Pre-market Exempt | false | 
| MRI Safety Status | MR Conditional | 
| Human Cell/Tissue Product | false | 
| Device Kit | false | 
| Device Combination Product | false | 
| Single Use | true | 
| Lot Batch | true | 
| Serial Number | false | 
| Manufacturing Date | true | 
| Expiration Date | true | 
| Donation Id Number | false | 
| Contains Natural Rubber Latex | false | 
| Labeled No Natural Rubber Latex | true | 
| RX Perscription | true | 
| 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 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Issuing Agency | Device ID | 
|---|---|
| GS1 | 00816777025999 [Primary] | 
| NJE | intracranial neurovascular stent | 
| Steralize Prior To Use | false | 
| Device Is Sterile | true | 
| Public Version Status | New | 
| Device Record Status | Published | 
| Public Version Number | 1 | 
| Public Version Date | 2018-12-26 | 
| Device Publish Date | 2018-11-25 | 
| Mark Image Registration | Serial | Company Trademark Application Date | 
|---|---|
|  LVIS  88292195  not registered Live/Pending | LVIS Corporation 2019-02-07 | 
|  LVIS  85040355  4376786 Live/Registered | MicroVention, Inc. 2010-05-17 | 
|  LVIS  77525463  not registered Dead/Abandoned | WISEDV, INC. 2008-07-17 | 
|  LVIS  77061891  not registered Dead/Abandoned | WiseDV Inc. 2006-12-11 | 
|  LVIS  74690735  not registered Dead/Abandoned | Princeton Electronic Billboard, Inc. 1995-06-19 | 
|  LVIS  74368612  1808955 Live/Registered | GENTEX CORPORATION 1993-03-17 |