Primary Device ID | 03700569654191 |
NIH Device Record Key | f69e0335-9b57-4f93-abb3-c3e9b81dd02b |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Footmotion Plating System |
Version Model Number | CAT2.8L42D |
Catalog Number | CAT2.8L42D |
Company DUNS | 263281904 |
Company Name | NEWCLIP TECHNICS |
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 | 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 | 03700569654191 [Primary] |
HWC | Screw, Fixation, Bone |
Steralize Prior To Use | true |
Device Is Sterile | false |
[03700569654191]
Moist Heat or Steam Sterilization
[03700569654191]
Moist Heat or Steam Sterilization
[03700569654191]
Moist Heat or Steam Sterilization
[03700569654191]
Moist Heat or Steam Sterilization
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-11-21 |
Device Publish Date | 2024-11-13 |