| Primary Device ID | 08806388297245 |
| NIH Device Record Key | eda47026-a6a2-41a9-99f6-b0252ce301ff |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | AnyOne Internal Fixture [Free sample] |
| Version Model Number | IF4510 |
| Catalog Number | M-IF4510C |
| Company DUNS | 687388178 |
| Company Name | Megagen Implant Co. Ltd |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | MR Conditional |
| 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 | 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 | 08806388297245 [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 | 2023-11-16 |
| Device Publish Date | 2023-11-08 |
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| 08800292994870 - MUA Scanbody Kit for R2 Photogram | 2026-02-16 |
| 08800293009894 - R2 Photogram | 2026-02-16 |
| 08800293009979 - AXA Scanbody for R2 Phtogram | 2026-02-16 |
| 08800293009986 - MUA Scanbody for R2 Photogram | 2026-02-16 |
| 08800292993453 - i-Peg | 2026-01-01 |
| 08800292993460 - i-Peg | 2026-01-01 |
| 08800292993477 - i-Peg | 2026-01-01 |