Primary Device ID | 08809987230941 |
NIH Device Record Key | 4d0f2834-2424-45eb-9e5b-a410facba695 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Peridot-TD Intervertebral body fusion system |
Version Model Number | L431-0030S |
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 | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | false |