Primary Device ID | 08800113300552 |
NIH Device Record Key | 122246c2-a6c3-4005-8bfc-422bbaa7c2c6 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Peridot Anterior Cervical Intervertebral Body Fusion System |
Version Model Number | C24F-2015 |
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 | 08800113300552 [Primary] |
ODP | Intervertebral Fusion Device With Bone Graft, Cervical |
Steralize Prior To Use | true |
Device Is Sterile | false |
[08800113300552]
Moist Heat or Steam Sterilization
[08800113300552]
Moist Heat or Steam Sterilization
[08800113300552]
Moist Heat or Steam Sterilization
[08800113300552]
Moist Heat or Steam Sterilization
[08800113300552]
Moist Heat or Steam Sterilization
[08800113300552]
Moist Heat or Steam Sterilization
[08800113300552]
Moist Heat or Steam Sterilization
[08800113300552]
Moist Heat or Steam Sterilization
[08800113300552]
Moist Heat or Steam Sterilization
[08800113300552]
Moist Heat or Steam Sterilization
[08800113300552]
Moist Heat or Steam Sterilization
[08800113300552]
Moist Heat or Steam Sterilization
[08800113300552]
Moist Heat or Steam Sterilization
[08800113300552]
Moist Heat or Steam Sterilization
[08800113300552]
Moist Heat or Steam Sterilization
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2021-05-10 |
Device Publish Date | 2021-04-30 |