| Primary Device ID | 06970575220124 |
| NIH Device Record Key | 2627d1ab-bc84-4e51-b84d-19ab32cacccc |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | KD |
| Version Model Number | PL001-3003 |
| Company DUNS | 544250984 |
| Company Name | SUZHOU KD INTELLIGENT DEVICE CO., LTD |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| 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 | true |
| Manufacturing Date | true |
| Expiration Date | true |
| 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 | 06970575220124 [Primary] |
| ITI | Wheelchair, Powered |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2024-05-22 |
| Device Publish Date | 2024-05-14 |
| 06970575220179 | PL001-3005 |
| 06970575220162 | PL001-4001 |
| 06970575220155 | PL001-7003 |
| 06970575220148 | PL001-7002 |
| 06970575220124 | PL001-3003 |
| 06970575220117 | PL001-2004 |
| 06970575220100 | PL001-2010 |
| 06970575220094 | PL001-2003 |
| 06970575220087 | PL001-8002 |
| 06970575220186 | PL001-8000 |
| 06970575220131 | PL001-7000 |
| 06970575220070 | PL001-6000 |
| 06970575220063 | PL001-5000 |
| 06970575220056 | PL001-4000 |
| 06970575220049 | PL001-3000 |
| 06970575220032 | PL001-2000 |
| 06970575220025 | PL001-1000 |
| 06970575220018 | PL001 |