| Primary Device ID | 08806388203499 |
| NIH Device Record Key | a91c6abc-bee3-4a55-82ce-f95b3e94752f |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Temporary Cylinder |
| Version Model Number | AANOTCO4010 |
| Catalog Number | AANOTCO4010T |
| Company DUNS | 687388178 |
| Company Name | Megagen Implant 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 | 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 | 08806388203499 [Primary] |
| NHA | Abutment, Implant, Dental, Endosseous |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[08806388203499]
Moist Heat or Steam Sterilization
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 5 |
| Public Version Date | 2019-11-08 |
| Device Publish Date | 2015-06-24 |
| 08806388203512 | AnyRidge Internal Ø5.8/ Octa |
| 08806388203505 | AnyRidge Internal Ø4.8/ Octa |
| 08806388203499 | AnyRidge Internal Ø3.8/ Octa |
| 08806388203482 | AnyRidge Internal Ø5.8/ Non-Octa |
| 08806388203475 | AnyRidge Internal Ø4.8/ Non-Octa |
| 08806388203468 | AnyRidge Internal Ø3.8/ Non-Octa |
| 08806388244102 | Ø4.8 / L=10 |
| 08809985656736 | Common |
| 08809985656729 | Common |
| 08809985656712 | Common |
| 08809985653469 | Common |
| 08809985653452 | Common |
| 08809977450496 | Common |
| 08809977450489 | Common |
| 08809977450472 | Common |
| 08809977450465 | Common |
| 08809985666063 | Ø5/ H=4/ Single |
| 08809985666001 | Ø5/ H=4/ Single |