| Primary Device ID | 08800026101130 |
| NIH Device Record Key | 9602813b-3099-48ba-8b66-adda2c8108b2 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | UT Fixture |
| Version Model Number | FUT43130 |
| Company DUNS | 688857820 |
| Company Name | WARANTEC.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 | true |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | true |
| Expiration Date | true |
| 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 | 08800026101130 [Primary] |
| DZE | Implant, Endosseous, Root-Form |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2023-04-20 |
| Device Publish Date | 2023-04-12 |
| 08800026101277 | FUT63115 |
| 08800026101260 | FUT63100 |
| 08800026101253 | FUT63085 |
| 08800026101246 | FUT63070 |
| 08800026101239 | FUT53130 |
| 08800026101222 | FUT53115 |
| 08800026101215 | FUT53100 |
| 08800026101208 | FUT53085 |
| 08800026101192 | FUT53070 |
| 08800026101185 | FUT48130 |
| 08800026101178 | FUT48115 |
| 08800026101161 | FUT48100 |
| 08800026101154 | FUT48085 |
| 08800026101147 | FUT48070 |
| 08800026101130 | FUT43130 |
| 08800026101123 | FUT43115 |
| 08800026101116 | FUT43100 |
| 08800026101109 | FUT43085 |
| 08800026101093 | FUT43070 |