| Primary Device ID | 04582276054919 |
| NIH Device Record Key | fd2f2153-1f3f-4fc1-a954-244ffb3698b5 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | SOLUUT PX ANTERIOR |
| Version Model Number | LS4, B1 |
| Company DUNS | 693430001 |
| Company Name | YAMAHACHI DENTAL MFG.,CO. |
| 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 | true |
| 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 | true |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 04582276054919 [Primary] |
| ELM | Denture, Plastic, Teeth |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2018-07-06 |
| Device Publish Date | 2018-02-06 |
| 04582276058405 | T7, A1 |
| 04582276058221 | T6, A1 |
| 04582276058047 | T5, A1 |
| 04582276057866 | T4, A1 |
| 04582276057651 | SS7, A1 |
| 04582276057477 | SS6, A1 |
| 04582276057293 | SS5, A1 |
| 04582276057118 | SS4, A1 |
| 04582276056906 | S7, A1 |
| 04582276056722 | S6, A1 |
| 04582276056548 | S5, A1 |
| 04582276056364 | S4, A1 |
| 04582276055046 | LS5, A1 |
| 04582276054919 | LS4, B1 |
| 04582276054704 | L7, B1 |
| 04582276054155 | L4, A4 |
| 04582276053004 | C6, A1 |
| 04582276052847 | C5, A3 |
| 04582276052823 | C5, A1 |
| 04582276055213 | LS5, W0.5 |
| 04582276053356 | C7, W0.5 |