| Primary Device ID | 08806388297108 | 
| NIH Device Record Key | a8f17669-9d08-4555-8358-927834d93e89 | 
| Commercial Distribution Status | In Commercial Distribution | 
| Brand Name | Lance Drill | 
| Version Model Number | LD1618L | 
| Catalog Number | LD1618L | 
| 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 | 08806388297108 [Primary] | 
| NDP | Accessories, Implant, Dental, Endosseous | 
| Steralize Prior To Use | true | 
| Device Is Sterile | false | 
[08806388297108]
Moist Heat or Steam Sterilization
| Public Version Status | Update | 
| Device Record Status | Published | 
| Public Version Number | 2 | 
| Public Version Date | 2020-01-09 | 
| Device Publish Date | 2019-11-29 | 
| 08806388297108 | Ø1.6/ L=18/ Long | 
| 08806388297092 | Ø1.6/ L=18/ Medium | 
| 08806388297085 | Ø1.6/ L=18/ Short | 
| 08806388285976 | Ø2/ L=37 | 
| 08806388237166 | Common Ø2.1/ L=7 | 
| 08806388226214 | Common Ø2/ L=15/ Long | 
| 08809728996655 | Common Ø2.0/ L=18/ Long | 
| 08809728996631 | Common Ø2.0/ L=18/ Short | 
| 08809931180247 | ARi ExCon Implant System | 
| 08809931180230 | ARi ExCon Implant System | 
| 08809931180223 | ARi ExCon Implant System | 
| 08800293008095 | Ø2.0/ L=13 | 
| 08800293008088 | Ø2.0/ L=11.5 | 
| 08800293008071 | Ø2.0/ L=6 | 
| 08800293008064 | Ø2/ L=46.5 |