Primary Device ID | 05056136800255 |
NIH Device Record Key | e22ef9b3-32a6-41e2-adb7-e96378720ba7 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Acorn 180 Stairlift |
Version Model Number | A180 |
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 | 05056136800255 [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 |