Primary Device ID | 00810028395169 |
NIH Device Record Key | 437afe14-beba-4125-8b14-9fefae5817c8 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | 5" K-Wire Tube |
Version Model Number | 211-99-007 |
Company DUNS | 828829072 |
Company Name | Trilliant Surgical, LLC |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
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 | false |
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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00810028395169 [Primary] |
HWC | Screw, Fixation, Bone |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00810028395169]
Moist Heat or Steam Sterilization
[00810028395169]
Moist Heat or Steam Sterilization
[00810028395169]
Moist Heat or Steam Sterilization
[00810028395169]
Moist Heat or Steam Sterilization
[00810028395169]
Moist Heat or Steam Sterilization
[00810028395169]
Moist Heat or Steam Sterilization
[00810028395169]
Moist Heat or Steam Sterilization
[00810028395169]
Moist Heat or Steam Sterilization
[00810028395169]
Moist Heat or Steam Sterilization
[00810028395169]
Moist Heat or Steam Sterilization
[00810028395169]
Moist Heat or Steam Sterilization
[00810028395169]
Moist Heat or Steam Sterilization
[00810028395169]
Moist Heat or Steam Sterilization
[00810028395169]
Moist Heat or Steam Sterilization
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-06-17 |
Device Publish Date | 2024-06-07 |