| Primary Device ID | 00889024683969 |
| NIH Device Record Key | 174e65e1-bd43-4307-9bdd-1030120c784d |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | G7® Revision Acetabular System |
| Version Model Number | 770000003 |
| Catalog Number | 770000003 |
| Company DUNS | 056038268 |
| Company Name | Zimmer, Inc. |
| 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 | false |
| 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 |
| Phone | +1(800)348-2759 |
| zimmer.consumerrelations@zimmerbiomet.com | |
| Phone | +1(800)348-2759 |
| zimmer.consumerrelations@zimmerbiomet.com |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00889024683969 [Primary] |
| HTD | FORCEPS |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2026-02-04 |
| Device Publish Date | 2025-11-03 |
| 00889024683969 - G7® Revision Acetabular System | 2026-02-04 |
| 00889024683969 - G7® Revision Acetabular System | 2026-02-04 |
| 00889024705524 - Identity 40MM Inset Humeral Protector | 2026-01-26 |
| 00889024705579 - 40mm Head Pusher | 2026-01-26 |
| 00889024693012 - Left 3 Deg Tib Cut Guide Assy | 2025-12-26 |
| 00889024693029 - Right 3 Deg Tib Cut Guide Assy | 2025-12-26 |
| 00889024703445 - TM Ankle Burr Guard C Large | 2025-12-26 |
| 00889024703872 - Offset Box Osteotome | 2025-12-26 |
| 00889024704008 - LB Type 1 Taper Extraction Insert | 2025-12-26 |