| Primary Device ID | 08806388206513 |
| NIH Device Record Key | cff727bd-d165-4e84-8aff-cfe06f57dc8d |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Stent Anchor |
| Version Model Number | AGSAW18 |
| Catalog Number | AGSAW18 |
| Company DUNS | 687388178 |
| Company Name | Megagen Implant Co. Ltd |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | true |
| MRI Safety Status | Labeling does not contain MRI Safety Information |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | false |
| Lot Batch | true |
| Serial Number | true |
| Manufacturing Date | true |
| Expiration Date | false |
| 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 | 08806388206513 [Primary] |
| NDP | Accessories, Implant, Dental, Endosseous |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[08806388206513]
Moist Heat or Steam Sterilization
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 4 |
| Public Version Date | 2020-01-09 |
| Device Publish Date | 2015-06-26 |
| 08806388206520 | AnyOne Internal M2.0/ Wide |
| 08806388206513 | AnyRidge Internal M1.8/ Wide |
| 08806388206506 | AnyOne Internal M2.0/ Regular |
| 08806388206490 | AnyRidge Internal M1.8/ Regular |
| 08809728993456 | BLUEDIAMOND M1.6/ RC/ Regular |
| 08809728993449 | BLUEDIAMOND M1.6/ NC/ Regular |
| 08809728993463 | BLUEDIAMOND Implant System M1.6/ RC/ Wide |
| 08809728993432 | M1.6/ NC/ Narrow |