| Primary Device ID | 06947600314868 |
| NIH Device Record Key | 5f4d0857-8a07-4058-96b8-b1104f05279e |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Implant, Regular |
| Version Model Number | 313020G |
| Company DUNS | 527603266 |
| Company Name | BIO CONCEPT 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 | 06947600314868 [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 | 2024-11-29 |
| Device Publish Date | 2024-11-21 |
| 06947600317999 | 316060G |
| 06947600317982 | 316050G |
| 06947600317975 | 316040G |
| 06947600317968 | 316030G |
| 06947600317951 | 316020G |
| 06947600317944 | 315060G |
| 06947600317937 | 315050G |
| 06947600317920 | 315040G |
| 06947600317913 | 315030G |
| 06947600317906 | 315020G |
| 06947600314967 | 314070G |
| 06947600314950 | 314060G |
| 06947600314943 | 314050G |
| 06947600314936 | 314040G |
| 06947600314929 | 314030G |
| 06947600314912 | 314020G |
| 06947600314905 | 313060G |
| 06947600314899 | 313050G |
| 06947600314882 | 313040G |
| 06947600314875 | 313030G |
| 06947600314868 | 313020G |
| 06947600314851 | 313010G |
| 06947600314844 | 312060G |
| 06947600314837 | 312020G |
| 06947600314820 | 312010G |
| 06947600314776 | 312050G |
| 06947600314721 | 312040G |
| 06947600314714 | 312030G |