| Primary Device ID | 04712771504750 |
| NIH Device Record Key | 086f6093-24f9-4e2c-b879-dd9ceb0dca16 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Ti Cancellous Screw |
| Version Model Number | 5206-1045 |
| Catalog Number | 5206-1045 |
| 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 |
| Length | 45 Millimeter |
| Device Size Text, specify | 0 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 04712771504750 [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 | 2018-08-07 |
| Device Publish Date | 2015-10-24 |
| 04712771504781 | Ti Cancellous Screw, Ø6.5 x 60mm |
| 04712771504774 | Ti Cancellous Screw, Ø6.5 x 55mm |
| 04712771504767 | Ti Cancellous Screw, Ø6.5 x 50mm |
| 04712771504750 | Ti Cancellous Screw, Ø6.5 x 45mm |
| 04712771504743 | Ti Cancellous Screw, Ø6.5 x 40mm |
| 04712771504736 | Ti Cancellous Screw, Ø6.5 x 35mm |
| 04712771504729 | Ti Cancellous Screw, Ø6.5 x 30mm |
| 04712771504712 | Ti Cancellous Screw, Ø6.5 x 25mm |
| 04712771504705 | Ti Cancellous Screw, Ø6.5 x20mm |
| 04712771504699 | Ti Cancellous Screw, Ø6.5 x 15mm |