| Primary Device ID | 08800018422502 |
| NIH Device Record Key | b24e7d0f-6a09-4ed4-850c-da2d4f7bd014 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | LLD 86 Basic |
| Version Model Number | LLD 86 Basic |
| Company DUNS | 689842626 |
| Company Name | DRTECH Corporation |
| 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 | 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 | 08800018422502 [Primary] |
| IXY | Holder, Radiographic Cassette, Wall-Mounted |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2024-05-16 |
| Device Publish Date | 2024-05-08 |
| 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 |