| Primary Device ID | 00817650020087 | 
| NIH Device Record Key | 0690ce0f-1446-4784-abc9-c3cc7cff52af | 
| Commercial Distribution Status | In Commercial Distribution | 
| Brand Name | Sierra | 
| Version Model Number | Sierra indoor | 
| Catalog Number | IL500 | 
| Company DUNS | 144008062 | 
| Company Name | HARMAR SUMMIT, LLC | 
| Device Count | 1 | 
| DM Exempt | false | 
| Pre-market Exempt | true | 
| 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 | false | 
| Serial Number | true | 
| Manufacturing Date | true | 
| 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 | 
| Phone | +1(800)833-0478 | 
| quality_team@harmar.com | |
| Phone | +1(800)833-0478 | 
| quality_team@harmar.com | |
| Phone | +1(800)833-0478 | 
| quality_team@harmar.com | |
| Phone | +1(800)833-0478 | 
| quality_team@harmar.com | |
| Phone | +1(800)833-0478 | 
| quality_team@harmar.com | |
| Phone | +1(800)833-0478 | 
| quality_team@harmar.com | |
| Phone | +1(800)833-0478 | 
| quality_team@harmar.com | |
| Phone | +1(800)833-0478 | 
| quality_team@harmar.com | |
| Phone | +1(800)833-0478 | 
| quality_team@harmar.com | |
| Phone | +1(800)833-0478 | 
| quality_team@harmar.com | |
| Phone | +1(800)833-0478 | 
| quality_team@harmar.com | |
| Phone | +1(800)833-0478 | 
| quality_team@harmar.com | |
| Phone | +1(800)833-0478 | 
| quality_team@harmar.com | |
| Phone | +1(800)833-0478 | 
| quality_team@harmar.com | |
| Phone | +1(800)833-0478 | 
| quality_team@harmar.com | |
| Phone | +1(800)833-0478 | 
| quality_team@harmar.com | |
| Phone | +1(800)833-0478 | 
| quality_team@harmar.com | |
| Phone | +1(800)833-0478 | 
| quality_team@harmar.com | |
| Phone | +1(800)833-0478 | 
| quality_team@harmar.com | 
| Device Issuing Agency | Device ID | 
|---|---|
| GS1 | 00817650020087 [Primary] | 
| PCE | Permanently mounted wheelchair platform lift | 
| Steralize Prior To Use | false | 
| Device Is Sterile | false | 
| Public Version Status | Update | 
| Device Record Status | Published | 
| Public Version Number | 2 | 
| Public Version Date | 2018-03-29 | 
| Device Publish Date | 2016-09-24 | 
| 00817650020094 | Incline stairway lift outdoor | 
| 00817650020087 | Incline stairway lift Indoor |