| Primary Device ID | 08806388234240 |
| NIH Device Record Key | 816bbc5b-ce6d-4d2c-a3a8-ba00fd453304 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Sinus Lift |
| Version Model Number | SCD3848 |
| Catalog Number | SCD3848 |
| 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 | 08806388234240 [Primary] |
| NDP | Accessories, Implant, Dental, Endosseous |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[08806388234240]
Moist Heat or Steam Sterilization
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 4 |
| Public Version Date | 2019-11-27 |
| Device Publish Date | 2015-06-23 |
| 08800292994900 - Impression Coping | 2025-10-03 Ø5/ H=4 |
| 08800292994948 - Temporary Abutment | 2025-10-03 |
| 08800292994955 - Temporary Abutment | 2025-10-03 |
| 08800292994962 - Temporary Abutment | 2025-10-03 |
| 08800292994979 - Temporary Abutment | 2025-10-03 |
| 08800292994986 - Temporary Abutment | 2025-10-03 |
| 08800292994993 - Temporary Abutment | 2025-10-03 |
| 08800292995006 - Tissue Punch | 2025-10-03 Ø3.3/ Narrow |