Primary Device ID | 08809282816765 |
NIH Device Record Key | a08c0272-ea0a-4189-a061-0423a1c827a2 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | ARIX System Bone Screw |
Version Model Number | 23-FC-010 |
Company DUNS | 688811603 |
Company Name | Jeil Medical Corporation |
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 | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 08809282816765 [Primary] |
HWC | Screw, Fixation, Bone |
Steralize Prior To Use | true |
Device Is Sterile | false |
[08809282816765]
Moist Heat or Steam Sterilization
[08809282816765]
Moist Heat or Steam Sterilization
[08809282816765]
Moist Heat or Steam Sterilization
[08809282816765]
Moist Heat or Steam Sterilization
[08809282816765]
Moist Heat or Steam Sterilization
[08809282816765]
Moist Heat or Steam Sterilization
[08809282816765]
Moist Heat or Steam Sterilization
[08809282816765]
Moist Heat or Steam Sterilization
[08809282816765]
Moist Heat or Steam Sterilization
[08809282816765]
Moist Heat or Steam Sterilization
[08809282816765]
Moist Heat or Steam Sterilization
[08809282816765]
Moist Heat or Steam Sterilization
[08809282816765]
Moist Heat or Steam Sterilization
[08809282816765]
Moist Heat or Steam Sterilization
[08809282816765]
Moist Heat or Steam Sterilization
[08809282816765]
Moist Heat or Steam Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 7 |
Public Version Date | 2024-05-31 |
Device Publish Date | 2015-09-24 |