| Primary Device ID | 00889024012080 |
| NIH Device Record Key | 07d8e86d-f3ab-4b97-a141-5a8cf958251f |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Tapered Screw-Vent® Implant System |
| Version Model Number | 15AT434 |
| 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 Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00889024012080 [Primary] |
| NHA | ABUTMENT, IMPLANT, DENTAL, ENDOSSEOUS |
| 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 | 2015-10-21 |
| 00889024021556 | ZRA462A |
| 00889024021549 | ZRA461A |
| 00889024021532 | ZRA452S |
| 00889024021525 | ZRA451S |
| 00889024021518 | ZRA352A |
| 00889024021501 | ZRA351A |
| 00889024021495 | ZRA342S |
| 00889024021488 | ZRA341S |
| 00889024019140 | TSI4 |
| 00889024019133 | TSI1 |
| 00889024019119 | TSCW |
| 00889024019102 | TSC5 |
| 00889024019096 | TSC |
| 00889024019089 | TSB25 |
| 00889024018495 | TACW5 |
| 00889024018488 | TACW4 |
| 00889024018471 | TACW3 |
| 00889024018464 | TACW2 |
| 00889024018457 | TACW1 |
| 00889024018440 | TAC5 |
| 00889024018433 | TAC4 |
| 00889024018426 | TAC3 |
| 00889024018419 | TAC2 |
| 00889024018402 | TAC1 |
| 00889024018396 | TA5C4 |
| 00889024018389 | TA5C3 |
| 00889024018372 | TA5C2 |
| 00889024018365 | TA5C1 |
| 00889024017108 | SCTS |
| 00889024016293 | PSATH4RF |
| 00889024016231 | PSATH3RM |
| 00889024016217 | PSATH3RF |
| 00889024015661 | NEA4G |
| 00889024015654 | NEA3G |
| 00889024015258 | HLA5G |
| 00889024015234 | HLA4G |
| 00889024015197 | HLA3G |
| 00889024015128 | HC565 |
| 00889024015111 | HC563 |
| 00889024015104 | HC465 |
| 00889024015098 | HC463 |
| 00889024015081 | HC457 |
| 00889024015074 | HC455 |
| 00889024014640 | DHTS2 |
| 00889024014633 | DHTS |
| 00889024014299 | CAN |
| 00889024014268 | CAB |
| 00889024014213 | BACW6 |
| 00889024014206 | BACW4 |
| 00889024014190 | BACW2 |