| Primary Device ID | 00889024109841 |
| NIH Device Record Key | 57d30d9d-d22c-4bae-ab34-44d0af7ee0cb |
| Commercial Distribution Status | In Commercial Distribution |
| Version Model Number | 28.30.150 |
| Company DUNS | 488133448 |
| Company Name | Zimmer GmbH |
| Device Count | 1 |
| DM Exempt | true |
| 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 | 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@zimmer.com | |
| Phone | 1(800)348-2759 |
| zimmer.consumerrelations@zimmer.com |
| Length | 50 Millimeter |
| Length | 50 Millimeter |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00889024109841 [Primary] |
| HRS | Plate, Fixation, Bone |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[00889024109841]
Moist Heat or Steam Sterilization
[00889024109841]
Moist Heat or Steam Sterilization
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2018-07-06 |
| Device Publish Date | 2016-08-29 |
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| 00889024593190 - Wagner Cone Prosthesis® | 2023-12-20 |
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| 00889024593213 - Wagner Cone Prosthesis® | 2023-12-20 |
| 00889024593237 - Wagner Cone Prosthesis® | 2023-12-20 |
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