| Primary Device ID | 08800026101062 |
| NIH Device Record Key | 821ae51d-945f-40b6-aa2b-dc6885f56546 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | IU Fixture |
| Version Model Number | FIU60070 |
| 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 | 08800026101062 [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 |
| 08800026101086 | FIU60100 |
| 08800026101079 | FIU60085 |
| 08800026101062 | FIU60070 |
| 08800026101055 | FIU55130 |
| 08800026101048 | FIU55115 |
| 08800026101031 | FIU55100 |
| 08800026101024 | FIU55085 |
| 08800026101017 | FIU55070 |
| 08800026101000 | FIU50130 |
| 08800026100997 | FIU50115 |
| 08800026100980 | FIU50100 |
| 08800026100973 | FIU50085 |
| 08800026100966 | FIU50070 |
| 08800026100959 | FIU45130 |
| 08800026100942 | FIU45115 |
| 08800026100935 | FIU45100 |
| 08800026100928 | FIU45085 |
| 08800026100911 | FIU45070 |
| 08800026100904 | FIU40130 |
| 08800026100898 | FIU40115 |
| 08800026100881 | FIU40100 |
| 08800026100874 | FIU40085 |
| 08800026100867 | FIU40070 |
| 08800026100850 | FIU36130 |
| 08800026100843 | FIU36115 |
| 08800026100836 | FIU36100 |
| 08800026100829 | FIU36085 |