| Primary Device ID | 00889024051850 |
| NIH Device Record Key | 39dd8325-f09f-4000-9610-5797f3a40996 |
| Commercial Distribution Status | In Commercial Distribution |
| Version Model Number | 2347-20-50 |
| Catalog Number | 00-2347-020-50 |
| 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 | 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 |
| Length | 50 Millimeter |
| Device Size Text, specify | 0 |
| Length | 50 Millimeter |
| Device Size Text, specify | 0 |
| Length | 50 Millimeter |
| Device Size Text, specify | 0 |
| Length | 50 Millimeter |
| Device Size Text, specify | 0 |
| Length | 50 Millimeter |
| Device Size Text, specify | 0 |
| Length | 50 Millimeter |
| Device Size Text, specify | 0 |
| Length | 50 Millimeter |
| Device Size Text, specify | 0 |
| Length | 50 Millimeter |
| Device Size Text, specify | 0 |
| Length | 50 Millimeter |
| Device Size Text, specify | 0 |
| Length | 50 Millimeter |
| Device Size Text, specify | 0 |
| Length | 50 Millimeter |
| Device Size Text, specify | 0 |
| Length | 50 Millimeter |
| Device Size Text, specify | 0 |
| Length | 50 Millimeter |
| Device Size Text, specify | 0 |
| Length | 50 Millimeter |
| Device Size Text, specify | 0 |
| Length | 50 Millimeter |
| Device Size Text, specify | 0 |
| Length | 50 Millimeter |
| Device Size Text, specify | 0 |
| Length | 50 Millimeter |
| Device Size Text, specify | 0 |
| Length | 50 Millimeter |
| Device Size Text, specify | 0 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00889024051850 [Primary] |
| HWC | Screw, fixation, bone |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[00889024051850]
Moist Heat or Steam Sterilization
[00889024051850]
Moist Heat or Steam Sterilization
[00889024051850]
Moist Heat or Steam Sterilization
[00889024051850]
Moist Heat or Steam Sterilization
[00889024051850]
Moist Heat or Steam Sterilization
[00889024051850]
Moist Heat or Steam Sterilization
[00889024051850]
Moist Heat or Steam Sterilization
[00889024051850]
Moist Heat or Steam Sterilization
[00889024051850]
Moist Heat or Steam Sterilization
[00889024051850]
Moist Heat or Steam Sterilization
[00889024051850]
Moist Heat or Steam Sterilization
[00889024051850]
Moist Heat or Steam Sterilization
[00889024051850]
Moist Heat or Steam Sterilization
[00889024051850]
Moist Heat or Steam Sterilization
[00889024051850]
Moist Heat or Steam Sterilization
[00889024051850]
Moist Heat or Steam Sterilization
[00889024051850]
Moist Heat or Steam Sterilization
[00889024051850]
Moist Heat or Steam Sterilization
[00889024051850]
Moist Heat or Steam Sterilization
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2019-12-10 |
| Device Publish Date | 2015-10-12 |
| 00889024691315 - Identity Humeral | 2025-09-30 |
| 00889024691353 - Identity Humeral | 2025-09-30 |
| 00889024691476 - Identity Humeral | 2025-09-30 |
| 00889024691551 - Identity Humeral | 2025-09-30 |
| 00889024691582 - Identity Humeral | 2025-09-30 |
| 00889024691681 - Identity Humeral | 2025-09-30 |
| 00889024691728 - Identity Humeral | 2025-09-30 |
| 00889024691919 - Identity Humeral | 2025-09-30 |