| Primary Device ID | 00889024020221 |
| NIH Device Record Key | b31b180e-f896-44e7-b159-d867deb63196 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Tapered Screw-Vent AdVent SwissPlus Implant Systems |
| Version Model Number | URS2 |
| Company DUNS | 103167086 |
| Company Name | ZIMMER DENTAL INC. |
| Device Count | 1 |
| DM Exempt | true |
| Pre-market Exempt | false |
| MRI Safety Status | Labeling does not contain MRI Safety Information |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | true |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | false |
| Expiration Date | true |
| 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 | 00889024020221 [Primary] |
| DZE | IMPLANT, ENDOSSEOUS, ROOT-FORM |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 5 |
| Public Version Date | 2019-11-08 |
| Device Publish Date | 2015-10-23 |
| 00889024017788 - Driva | 2023-07-17 STEP DRILL,3.8/3.4MM,25MM |
| 00889024015890 - Tapered SwissPlus® & SwisPlus® | 2023-06-29 |
| 00889024015630 - N/A | 2021-03-10 |
| 00889024010949 - Tapered Screw-Vent® Screw-Vent® AdVent® Tapered SwissPlus® Spline® | 2020-03-23 |
| 00889024010956 - Integral® | 2020-03-23 |
| 00889024010963 - Spline® | 2020-03-23 |
| 00889024010970 - Spline® | 2020-03-23 |
| 00889024011496 - N/A | 2020-03-23 |