| Primary Device ID | 05420060310072 |
| NIH Device Record Key | dc663879-bf75-47b6-b36e-5d6e933df6f6 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Zimmer Biomet Patient Specific Instruments |
| Version Model Number | KNM-ZB11-00-01 |
| Catalog Number | KNM-ZB11-00-01 |
| Company DUNS | 373139427 |
| Company Name | Materialise NV |
| 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 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 05420060310072 [Primary] |
| OOG | Knee Arthroplasty Implantation System |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[05420060310072]
Moist Heat or Steam Sterilization
[05420060310072]
Moist Heat or Steam Sterilization
[05420060310072]
Moist Heat or Steam Sterilization
[05420060310072]
Moist Heat or Steam Sterilization
[05420060310072]
Moist Heat or Steam Sterilization
[05420060310072]
Moist Heat or Steam Sterilization
[05420060310072]
Moist Heat or Steam Sterilization
[05420060310072]
Moist Heat or Steam Sterilization
[05420060310072]
Moist Heat or Steam Sterilization
[05420060310072]
Moist Heat or Steam Sterilization
[05420060310072]
Moist Heat or Steam Sterilization
[05420060310072]
Moist Heat or Steam Sterilization
[05420060310072]
Moist Heat or Steam Sterilization
[05420060310072]
Moist Heat or Steam Sterilization
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2019-11-27 |
| Device Publish Date | 2018-08-11 |
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