| Primary Device ID | 08806388239672 |
| NIH Device Record Key | 5ee58031-c1da-48b8-8295-d5fbb0dfeb01 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Hand Tap |
| Version Model Number | THT250L |
| Catalog Number | THT250L |
| 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 | 08806388239672 [Primary] |
| NDP | Accessories, Implant, Dental, Endosseous |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[08806388239672]
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 | 2015-06-24 |
| 08806388239672 | Common M2.5 |
| 08806388239665 | Common M2 |
| 08806388239658 | AnyRidge Internal M1.8 |
| 08806388239641 | Common M1.6 |
| 08809985667749 | M2.0 |
| 08809985667732 | M2.0 |
| 08809985667725 | M2.0 |
| 08809985667718 | M2.0 |
| 08809985667701 | M1.8 |
| 08809985667695 | M1.8 |
| 08809985667688 | M1.8 |
| 08809985667671 | M1.8 |
| 08809985667664 | M1.6 |
| 08809985667657 | M1.6 |
| 08809985667640 | M1.6 |
| 08809985667633 | M1.6 |