| Primary Device ID | 08809488210169 |
| NIH Device Record Key | 81ad1bbd-c46d-4028-95c0-74dcb2ad422e |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | ANCHOR PLUS/NEO ANCHOR PLUS |
| Version Model Number | MSS-1406 |
| Company DUNS | 688476027 |
| Company Name | KJMEDITECH.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 | 08809488210169 [Primary] |
| DZE | Implant, Endosseous, Root-Form |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2024-01-03 |
| Device Publish Date | 2019-08-26 |
| 08809488210251 | MSS-1612 |
| 08809488210244 | MSS-1610 |
| 08809488210237 | MSS-1608 |
| 08809488210220 | MSS-1607 |
| 08809488210213 | MSS-1606 |
| 08809488210206 | MSS-1412 |
| 08809488210190 | MSS-1410 |
| 08809488210183 | MSS-1408 |
| 08809488210176 | MSS-1407 |
| 08809488210169 | MSS-1406 |
| 08809488210152 | MS-1612 |
| 08809488210145 | MS-1610 |
| 08809488210138 | MS-1608 |
| 08809488210121 | MS-1607 |
| 08809488210114 | MS-1606 |
| 08809488210107 | MS-1412 |
| 08809488210091 | MS-1410 |
| 08809488210084 | MS-1408 |
| 08809488210077 | MS-1407 |
| 08809488210060 | MS-1406 |