| Primary Device ID | 00889024144262 |
| NIH Device Record Key | 08ec623f-2ccc-47d4-acab-00d3b46d8947 |
| Commercial Distribution Status | In Commercial Distribution |
| Version Model Number | 8005-52 |
| Catalog Number | 00-8005-052-00 |
| Company DUNS | 056038268 |
| Company Name | Zimmer, Inc. |
| Device Count | 1 |
| DM Exempt | false |
| 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 |
| Phone | +1(800)348-2759 |
| zimmer.consumerrelations@zimmerbiomet.com |
| Outer Diameter | 56 Millimeter |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00889024144262 [Primary] |
| JDI | Prosthesis, hip, semi-constrained, metal/polymer, cemented |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 4 |
| Public Version Date | 2020-01-14 |
| Device Publish Date | 2015-09-17 |
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| 00889024670778 - TROCAR SCREW PIN DRIVER | 2024-05-21 |
| 00889024670907 - X SERIES POWER MODIFIED CASE | 2024-05-21 |
| 00889024671072 - TMR PLUS SEATING GAUGE | 2024-05-21 |
| 00889024660595 - BIOMET Anterior Adapter | 2024-04-23 |
| 00889024660601 - BIOMET Posterior Adapter | 2024-04-23 |
| 00889024660816 - +9MM Spacer Block C/D 10mm | 2024-04-23 |
| 00889024660823 - +9MM Spacer Block C/D 12mm | 2024-04-23 |