| Primary Device ID | 08800033801252 |
| NIH Device Record Key | d87e2a17-a65c-46f7-bf14-9b92179c25cd |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | The JASPER Spinal Fixation System |
| Version Model Number | L213-90110 |
| Company DUNS | 694609156 |
| Company Name | GBS Commonwealth Co.,Ltd. |
| 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 | true |
| Expiration Date | false |
| 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 | 08800033801252 [Primary] |
| NKB | Thoracolumbosacral Pedicle Screw System |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[08800033801252]
Moist Heat or Steam Sterilization
[08800033801252]
Moist Heat or Steam Sterilization
[08800033801252]
Moist Heat or Steam Sterilization
[08800033801252]
Moist Heat or Steam Sterilization
[08800033801252]
Moist Heat or Steam Sterilization
[08800033801252]
Moist Heat or Steam Sterilization
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2024-12-23 |
| Device Publish Date | 2019-08-23 |