Primary Device ID | 08800033842231 |
NIH Device Record Key | f43e27be-2ce8-4422-b0d0-f31e09bf2f5a |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | The JASPER Spinal Fixation System |
Version Model Number | L223-0060 |
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 |