| Primary Device ID | 08809977450649 |
| NIH Device Record Key | f2b7a7a9-fbb0-4536-baa4-0f29f5f74cb3 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Scan Cap |
| Version Model Number | AXSC504 |
| Catalog Number | AXSC504T |
| 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 | true |
| Lot Batch | true |
| Serial Number | true |
| Manufacturing Date | true |
| Expiration Date | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | true |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 08809977450649 [Primary] |
| NDP | Accessories, Implant, Dental, Endosseous |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[08809977450649]
Moist Heat or Steam Sterilization
[08809977450649]
Moist Heat or Steam Sterilization
[08809977450649]
Moist Heat or Steam Sterilization
[08809977450649]
Moist Heat or Steam Sterilization
[08809977450649]
Moist Heat or Steam Sterilization
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2024-07-18 |
| Device Publish Date | 2024-07-10 |
| 08809985659485 | Common |
| 08809985659478 | Common |
| 08809985659461 | Common |
| 08809985659454 | Common |
| 08809985659447 | Common |
| 08809985659430 | Common |
| 08809985659423 | Common |
| 08809985659416 | Common |
| 08809985656682 | Common |
| 08809977450670 | Common |
| 08809977450663 | Common |
| 08809977450656 | Common |
| 08809977450649 | AXSC504 |
| 08809977450632 | Common |
| 08809977450625 | AXSC404 |
| 08809985666216 | Ø5/ H=4 |
| 08809985666186 | Ø5/ H=4 |
| 08809985663307 | Ø5/ H=4 |