| Primary Device ID | 00889024520035 |
| NIH Device Record Key | 2929e5db-9163-4c3f-bae1-e3819864e6db |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | G7® Vivacit-E® |
| Version Model Number | 30104410 |
| Catalog Number | 30104410 |
| Company DUNS | 056038268 |
| Company Name | Zimmer, Inc. |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | MR Conditional |
| 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 |
| Phone | +1(800)348-2759 |
| zimmer.consumerrelations@zimmerbiomet.com |
| Lumen/Inner Diameter | 44 Millimeter |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00889024520035 [Primary] |
| OQG | Hip Prosthesis, semi-constrained, cemented, metal/polymer, + additive, porous, uncemented |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2020-01-08 |
| Device Publish Date | 2019-12-31 |