| Primary Device ID | 04711605569361 |
| NIH Device Record Key | 3a98bb00-82f5-442d-86b5-762314f15ee9 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | UCP Centralizer with cement restrictor |
| Version Model Number | 1907-3018 |
| Catalog Number | 1907-3018 |
| 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 | 04711605569361 [Primary] |
| LZO | Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 4 |
| Public Version Date | 2018-08-08 |
| Device Publish Date | 2016-03-31 |
| 04711605569361 | UCP Centralizer with cement restrictor, 18C |
| 04711605569354 | UCP Centralizer with cement restrictor, 16C |
| 04711605569347 | UCP Centralizer with cement restrictor, 14C |
| 04711605569330 | UCP Centralizer with cement restrictor, 12C |
| 04711605569323 | UCP Centralizer with cement restrictor, 10C |
| 04711605569316 | UCP Centralizer with cement restrictor, 8C |