| Primary Device ID | 10194346231420 |
| NIH Device Record Key | 5661e9b6-87aa-43b8-802d-e741e04e0787 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Parent's Choice |
| Version Model Number | K5101US |
| Company DUNS | 051957769 |
| Company Name | WAL-MART STORES, INC. |
| 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 | true |
| 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 | true |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00194346231423 [Primary] |
| GS1 | 10194346231420 [Package] Contains: 00194346231423 Package: [4 Units] In Commercial Distribution |
| GS1 | 20194346231427 [Package] Package: [6 Units] In Commercial Distribution |
| INB | Attachment, Commode, Wheelchair |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2024-11-06 |
| Device Publish Date | 2024-10-29 |