| Primary Device ID | 08800018408001 |
| NIH Device Record Key | 6ce4dad7-8219-4708-9718-b6c660652fa4 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | EXPD 4357P |
| Version Model Number | EXPD 4357P |
| Company DUNS | 689842626 |
| Company Name | DRTECH Corporation |
| 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 | false |
| 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 | true |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 08800018408001 [Primary] |
| MQB | Solid State X-Ray Imager (Flat Panel/Digital Imager) |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2023-09-12 |
| Device Publish Date | 2023-09-04 |
| 08800018422601 - EXTRON 3 | 2025-06-25 |
| 08800018430002 - EXPD-N series | 2025-06-23 |
| 08800018430101 - EXPD-N series | 2025-06-23 |
| 08800018430200 - EXPD-N series | 2025-06-23 |
| 08800018430309 - EXPD-N series | 2025-06-23 |
| 08800018430408 - EXPD-N series | 2025-06-23 |
| 08800018430507 - EXPD-N series | 2025-06-23 |
| 08800018430606 - EXPD-N series | 2025-06-23 |