| Primary Device ID | 09348215059095 |
| NIH Device Record Key | d5fa2b76-486c-4fcc-b044-54b3e910adec |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | PEEK RCI Screw |
| Version Model Number | 121-05-5230 |
| Company DUNS | 751993028 |
| Company Name | SIGNATURE ORTHOPAEDICS PTY LTD |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | MR Safe |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | true |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | true |
| Expiration Date | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | false |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 09348215059095 [Primary] |
| MBI | Fastener, Fixation, Nondegradable, Soft Tissue |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2023-06-05 |
| Device Publish Date | 2023-05-26 |
| 09348215082109 | 121-05-6271 |
| 09348215082093 | 121-05-6231 |
| 09348215082086 | 121-05-5231 |
| 09348215082079 | 121-05-2370 |
| 09348215082062 | 121-05-2320 |
| 09348215081881 | 121-05-1370 |
| 09348215081874 | 121-05-1320 |
| 09348215081867 | 121-05-0370 |
| 09348215059200 | 121-05-9370 |
| 09348215059194 | 121-05-9320 |
| 09348215059187 | 121-05-9270 |
| 09348215059170 | 121-05-8320 |
| 09348215059163 | 121-05-8270 |
| 09348215059156 | 121-05-8230 |
| 09348215059149 | 121-05-7320 |
| 09348215059132 | 121-05-7270 |
| 09348215059125 | 121-05-7230 |
| 09348215059118 | 121-05-6270 |
| 09348215059101 | 121-05-6230 |
| 09348215059095 | 121-05-5230 |
| 09348215122041 | 121-05-9271 |
| 09348215122034 | 121-05-8271 |
| 09348215122027 | 121-05-8231 |
| 09348215122010 | 121-05-7271 |
| 09348215122003 | 121-05-7231 |