| Primary Device ID | 04712602344500 |
| NIH Device Record Key | 6906f09c-2d5a-45db-b236-e45a7eb85a61 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | United Cement Restrictor |
| Version Model Number | 1905-7013 |
| Catalog Number | 1905-7013 |
| 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 | 04712602344500 [Primary] |
| LPH | Prosthesis, Hip, Semi-Constrained, Metal/Polymer, 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 | 2018-08-03 |
| Device Publish Date | 2015-10-24 |
| 04712602344531 | Cement Restrictor, Full PE, Ø16mm |
| 04712602344524 | Cement Restrictor, Full PE, Ø15mm |
| 04712602344517 | Cement Restrictor, Full PE, Ø14mm |
| 04712602344500 | Cement Restrictor, Full PE, Ø13mm |
| 04712602344494 | Cement Restrictor, Full PE, Ø12mm |
| 04712602344487 | Cement Restrictor, Full PE, Ø11mm |
| 04712602344470 | Cement Restrictor, Full PE, Ø10mm |
| 04712602344463 | Cement Restrictor, Full PE, Ø9mm |
| 04712602344456 | Cement Restrictor, Full PE, Ø8mm |
| 04712602344449 | Cement Restrictor, Full PE, Ø7mm |