| Primary Device ID | 05056136800095 |
| NIH Device Record Key | 592f1b2c-534f-458c-b7dd-528b483ecf03 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Acorn Stairlift |
| Version Model Number | Acorn 130 Perch Right Hand |
| 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 | 05056136800095 [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 | 2017-01-02 |
| 00505613680064 | Acorn 130 Outdoor Heavy Duty Left Hand |
| 05056136800217 | Acorn 180 Right Hand |
| 05056136800200 | Acorn 180 Left Hand |
| 05056136800095 | Acorn 130 Perch Right Hand |
| 05056136800088 | Acorn 130 Perch Left hand |
| 05056136800071 | Acorn 130 Outdoor Heavy Duty Right Hand |
| 05056136800057 | Acorn 130 Indoor Heavy Duty Right Hand |
| 05056136800040 | Acorn 130 Indoor Heavy Duty Left Hand |
| 05056136800033 | Acorn 130 Outdoor Right Hand |
| 05056136800026 | Acorn 130 Outdoor Left Hand |
| 05056136800019 | Acorn 130 Indoor Right Hand |
| 05056136800002 | Acorn 130 Indoor left Hand |