| Primary Device ID | 06975851430051 |
| NIH Device Record Key | 55a532ff-2f7d-4490-a549-435c4f57b716 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Xingfang |
| Version Model Number | XFE-8 |
| Company DUNS | 544323452 |
| Company Name | Hebei Xingfang Medical Instruments Technology Co.,Ltd |
| 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 | true |
| Manufacturing Date | true |
| 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 | 06975851430051 [Primary] |
| FNJ | Bed, Manual |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2023-08-04 |
| Device Publish Date | 2023-07-27 |
| 06975851430013 | XFA-5 |
| 06975851430150 | XFB-29 |
| 06975851430143 | XFB-21-3 |
| 06975851430136 | XFB-21-1 |
| 06975851430129 | XFB-16 |
| 06975851430112 | XFB-12 |
| 06975851430105 | XFB-11-1 |
| 06975851430099 | XFB-6 |
| 06975851430082 | XFB-10-1 |
| 06975851430075 | XFB-10 |
| 06975851430068 | XFA-5-2 |
| 06975851430396 | XFE-6 |
| 06975851430389 | XFE-5 |
| 06975851430372 | XFE-4 |
| 06975851430365 | XFE-3 |
| 06975851430174 | XFB-43-1 |
| 06975851430167 | XFB-42-1 |
| 06975851430051 | XFE-8 |
| 06975851430020 | XFB-45 |