| Primary Device ID | 05056136800248 |
| NIH Device Record Key | 15a094b9-a233-45a9-bbf8-9ec12184f8c7 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Acorn 130 Stairlift |
| Version Model Number | A130 |
| Company DUNS | 767086093 |
| Company Name | Acorn Stairlifts |
| Device Count | 1 |
| DM Exempt | true |
| 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 | 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 | 05056136800248 [Primary] |
| PCD | Powered Stairway Chair 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 | 2017-03-27 |
| 05056136800002 - Acorn Stairlift | 2018-03-29 |
| 05056136800019 - Acorn Stairlift | 2018-03-29 |
| 05056136800026 - Acorn Stairlift | 2018-03-29 |
| 05056136800033 - Acorn Stairlift | 2018-03-29 |
| 05056136800040 - Acorn Stairlift | 2018-03-29 |
| 05056136800057 - Acorn Stairlift | 2018-03-29 |
| 05056136800071 - Acorn Stairlift | 2018-03-29 |
| 05056136800088 - Acorn Stairlift | 2018-03-29 |