Primary Device ID | 08806388237166 |
NIH Device Record Key | 353a9c36-eae9-4bd0-a1df-e21aae4b4800 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Lance Drill |
Version Model Number | TANFLD2107 |
Catalog Number | TANFLD2107 |
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 | 08806388237166 [Primary] |
NDP | Accessories, Implant, Dental, Endosseous |
Steralize Prior To Use | true |
Device Is Sterile | false |
[08806388237166]
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 | 2015-06-23 |
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 |