| Primary Device ID | 04712602348904 |
| NIH Device Record Key | 97cffa73-0930-4d1b-8fb4-3edbda07ae6c |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Patellar, On set, 3 pegs |
| Version Model Number | 2403-1030 |
| Catalog Number | 2403-1030 |
| Company DUNS | 656700556 |
| Company Name | UNITED ORTHOPEDIC CORP. |
| 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 | +886229294567 |
| service@uoc.com.tw |
| Device Size Text, specify | 0 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 04712602348904 [Primary] |
| JWH | Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 4 |
| Public Version Date | 2018-07-13 |
| Device Publish Date | 2015-10-24 |
| 04712602348942 | Patellar, On set, 3 pegs, E-Larger, 44 mm |
| 04712602348935 | Patellar, On set, 3 pegs, XX-Larger, 41 mm |
| 04712602348928 | Patellar, On set, 3 pegs, X-Larger, 38 mm |
| 04712602348911 | Patellar, On set, 3 pegs, Larger, 35 mm |
| 04712602348904 | Patellar, On set, 3 pegs, Medium,32 mm |
| 04712602348898 | Patellar, On set, 3 pegs, Small, 29 mm |
| 04712602348881 | Patellar, On set, 3 pegs, X-Small, 26 mm |