| Primary Device ID | 08806388254040 |
| NIH Device Record Key | 7e4e5ab0-c07c-424e-b976-eef5fa054515 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Diamond Drill |
| Version Model Number | 2DD3025 |
| Catalog Number | 2DD3025 |
| 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 | 08806388254040 [Primary] |
| DZA | Drill, Dental, Intraoral |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[08806388254040]
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 | 2017-06-01 |
| 08806388254095 | Common Ø4/ L=5/ Tapered D |
| 08806388254088 | Common Ø2/ Final S |
| 08806388254071 | Common Ø5/ Final S |
| 08806388254064 | Common Ø3/ L=34/ Round D |
| 08806388254057 | Common Ø3/ L=29/ Round D |
| 08806388254040 | Common Ø3/ L=25/ Round D |
| 08806388254033 | Common Ø2/ L=34/ Round D |
| 08806388254026 | Common Ø2/ L=29/ Round D |
| 08806388254019 | Common Ø2/ L=25/ Round D |
| 08806388254002 | Common Ø1.9/ L=11/ Initial S |
| 08806388253999 | Common Ø1.6/ L=7/ Initial S |
| 08809708750727 | 3DD2008 |
| 08809977453299 | SLDD65L |
| 08809977453282 | SLDD65S |
| 08800293008101 | Ø3.3 |