| Primary Device ID | 00889024706217 |
| NIH Device Record Key | b36a33a7-04c8-4769-8a8a-ad47c1cbd09d |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Z1 BROACH SZ 12, HYBRID |
| Version Model Number | SSI008481 |
| Catalog Number | SSI008481 |
| 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 | false |
| Lot Batch | false |
| Serial Number | true |
| Manufacturing Date | false |
| 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 |
| 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 | 00889024706217 [Primary] |
| KWY | Prosthesis, Hip, Hemi-, Femoral, Metal/Polymer, Cemented Or Uncemented |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[00889024706217]
Moist Heat or Steam Sterilization
[00889024706217]
Moist Heat or Steam Sterilization
[00889024706217]
Moist Heat or Steam Sterilization
[00889024706217]
Moist Heat or Steam Sterilization
[00889024706217]
Moist Heat or Steam Sterilization
[00889024706217]
Moist Heat or Steam Sterilization
[00889024706217]
Moist Heat or Steam Sterilization
[00889024706217]
Moist Heat or Steam Sterilization
[00889024706217]
Moist Heat or Steam Sterilization
[00889024706217]
Moist Heat or Steam Sterilization
[00889024706217]
Moist Heat or Steam Sterilization
[00889024706217]
Moist Heat or Steam Sterilization
[00889024706217]
Moist Heat or Steam Sterilization
[00889024706217]
Moist Heat or Steam Sterilization
[00889024706217]
Moist Heat or Steam Sterilization
[00889024706217]
Moist Heat or Steam Sterilization
[00889024706217]
Moist Heat or Steam Sterilization
[00889024706217]
Moist Heat or Steam Sterilization
[00889024706217]
Moist Heat or Steam Sterilization
[00889024706217]
Moist Heat or Steam Sterilization
[00889024706217]
Moist Heat or Steam Sterilization
[00889024706217]
Moist Heat or Steam Sterilization
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2026-03-03 |
| Device Publish Date | 2026-02-23 |
| 00887868150876 - Affixus® | 2026-03-30 |
| 00887868150333 - Affixus® | 2026-03-27 |
| 00887868150340 - Affixus® | 2026-03-27 |
| 00887868150357 - Affixus® | 2026-03-27 |
| 00887868150364 - Affixus® | 2026-03-27 |
| 00887868150371 - Affixus® | 2026-03-27 |
| 00887868150388 - Affixus® | 2026-03-27 |
| 00887868150395 - Affixus® | 2026-03-27 |