| Primary Device ID | 05051995000181 |
| NIH Device Record Key | a3218060-40ff-4006-9d09-b4459bc6e5a6 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | QA3 Patient Stretcher System |
| Version Model Number | QA3 DRIVE Emergency Stretcher |
| Catalog Number | 21122 |
| Company DUNS | 083649158 |
| Company Name | Anetic Aid USA 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 | false |
| 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 | 05051995000181 [Primary] |
| FPO | Stretcher, Wheeled |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2023-09-19 |
| Device Publish Date | 2023-09-11 |
| 05051995008729 | QA3 Treatment Stretcher |
| 05051995008712 | QA3 DRIVE Powered Patient Stretcher |
| 05051995004912 | QA3 Ophthalmic Stretcher |
| 05051995000204 | QA3 Powered Emergency Stretcher |
| 05051995000198 | QA3 DRIVE Powered Emergency Stretcher |
| 05051995000181 | QA3 DRIVE Emergency Stretcher |
| 05051995000167 | QA3 DRIVE Powered Patient Stretcher |
| 05051995000150 | QA3 DRIVE Patient Stretcher |
| 05051995000013 | QA3 Emergency Stretcher |
| 05051995000006 | QA3 Patient Stretcher |