Primary Device ID | 08800167337542 |
NIH Device Record Key | bb0a88ed-3914-4be7-9b83-b1e5b69c6872 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Peridot-PT Anterior Cervical Intervertebral body fusion system |
Version Model Number | C417-1715S |
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 |