Primary Device ID | 08800113303652 |
NIH Device Record Key | be0f4be9-e0db-4a92-a0c9-381b54f80a21 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Peridot Anterior Cervical Intervertebral Body Fusion System |
Version Model Number | C220-1106 |
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 | 08800113303652 [Primary] |
ODP | Intervertebral Fusion Device With Bone Graft, Cervical |
Steralize Prior To Use | true |
Device Is Sterile | false |
[08800113303652]
Moist Heat or Steam Sterilization
[08800113303652]
Moist Heat or Steam Sterilization
[08800113303652]
Moist Heat or Steam Sterilization
[08800113303652]
Moist Heat or Steam Sterilization
[08800113303652]
Moist Heat or Steam Sterilization
[08800113303652]
Moist Heat or Steam Sterilization
[08800113303652]
Moist Heat or Steam Sterilization
[08800113303652]
Moist Heat or Steam Sterilization
[08800113303652]
Moist Heat or Steam Sterilization
[08800113303652]
Moist Heat or Steam Sterilization
[08800113303652]
Moist Heat or Steam Sterilization
[08800113303652]
Moist Heat or Steam Sterilization
[08800113303652]
Moist Heat or Steam Sterilization
[08800113303652]
Moist Heat or Steam Sterilization
[08800113303652]
Moist Heat or Steam Sterilization
[08800113303652]
Moist Heat or Steam Sterilization
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2021-04-08 |
Device Publish Date | 2021-03-31 |