| Primary Device ID | 08800056215920 |
| NIH Device Record Key | aae40ee6-b160-4a40-80cc-2acda8794da1 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Peridot Intervertebral body fusion system |
| Version Model Number | L351-D4A3 |
| 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 | 08800056215920 [Primary] |
| MAX | Intervertebral Fusion Device With Bone Graft, Lumbar |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[08800056215920]
Moist Heat or Steam Sterilization
[08800056215920]
Moist Heat or Steam Sterilization
[08800056215920]
Moist Heat or Steam Sterilization
[08800056215920]
Moist Heat or Steam Sterilization
[08800056215920]
Moist Heat or Steam Sterilization
[08800056215920]
Moist Heat or Steam Sterilization
[08800056215920]
Moist Heat or Steam Sterilization
[08800056215920]
Moist Heat or Steam Sterilization
[08800056215920]
Moist Heat or Steam Sterilization
[08800056215920]
Moist Heat or Steam Sterilization
[08800056215920]
Moist Heat or Steam Sterilization
[08800056215920]
Moist Heat or Steam Sterilization
[08800056215920]
Moist Heat or Steam Sterilization
[08800056215920]
Moist Heat or Steam Sterilization
[08800056215920]
Moist Heat or Steam Sterilization
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2020-06-08 |
| Device Publish Date | 2020-05-29 |