| Primary Device ID | 08800039325578 |
| NIH Device Record Key | 01a004d0-fa80-4f22-a80c-de49368fe912 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | IBS Implant System |
| Version Model Number | IBS6007 |
| Company DUNS | 631169224 |
| Company Name | InnoBioSurg Co.,Ltd(IBS implant Co.,Ltd) |
| Device Count | 1 |
| DM Exempt | true |
| Pre-market Exempt | false |
| MRI Safety Status | MR Unsafe |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | true |
| Lot Batch | true |
| Serial Number | true |
| Manufacturing Date | true |
| Expiration Date | true |
| Donation Id Number | true |
| 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 | 08800039325578 [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 | 2024-10-16 |
| Device Publish Date | 2024-10-08 |
| 08800039325448 | IBS4511 |
| 08800039325431 | IBS4509 |
| 08800039325424 | IBS4507 |
| 08800039325417 | IBS4015 |
| 08800039325400 | IBS4013 |
| 08800039325394 | IBS4011 |
| 08800039325387 | IBS4009 |
| 08800039325370 | IBS4007 |
| 08800039325615 | IBS6015 |
| 08800039325608 | IBS6013 |
| 08800039325592 | IBS6011 |
| 08800039325585 | IBS6009 |
| 08800039325578 | IBS6007 |
| 08800039325561 | IBS5515 |
| 08800039325554 | IBS5513 |
| 08800039325547 | IBS5511 |
| 08800039325530 | IBS5509 |
| 08800039325523 | IBS5507 |
| 08800039325516 | IBS5015 |
| 08800039325509 | IBS5013 |
| 08800039325493 | IBS5011 |
| 08800039325486 | IBS5009 |
| 08800039325479 | IBS5007 |
| 08800039325462 | IBS4515 |
| 08800039325455 | IBS4513 |