Primary Device ID | 00841731135155 |
NIH Device Record Key | 5e69cbee-3e18-4b27-a5aa-fbfe2b4b59fd |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | REDEMPTION DUO Nail System |
Version Model Number | RD-TARG-DT |
Catalog Number | RD-TARG-DT |
Company DUNS | 117502293 |
Company Name | VILEX LLC |
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 | false |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
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 | 00841731135155 [Primary] |
HSB | Rod, Fixation, Intramedullary And Accessories |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00841731135155]
Moist Heat or Steam Sterilization
[00841731135155]
Moist Heat or Steam Sterilization
[00841731135155]
Moist Heat or Steam Sterilization
[00841731135155]
Moist Heat or Steam Sterilization
[00841731135155]
Moist Heat or Steam Sterilization
[00841731135155]
Moist Heat or Steam Sterilization
[00841731135155]
Moist Heat or Steam Sterilization
[00841731135155]
Moist Heat or Steam Sterilization
[00841731135155]
Moist Heat or Steam Sterilization
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-11-20 |
Device Publish Date | 2024-11-12 |
00841731142528 | REDEMPTION DUO Insertion Tool |
00841731135537 | REDEMPTION DUO Proximal Guide Extender |
00841731135186 | REDEMPTION DUO Heel Cup Assembly |
00841731135162 | REDEMPTION DUO Nail Attachment Rod |
00841731135155 | REDEMPTION DUO Distal Arm Assembly |
00841731135148 | REDEMPTION DUO Proximal Arm Assembly |