Primary Device ID | 04560224971501 |
NIH Device Record Key | 1ad8e5e8-d142-4813-8110-538475b0ebf7 |
Commercial Distribution Discontinuation | 2022-09-23 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | FC |
Version Model Number | FC |
Company DUNS | 690710546 |
Company Name | NAKANISHI INC. |
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 | false |
Serial Number | true |
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 | 04560224971501 [Primary] |
EKX | Handpiece, direct drive, ac-powered |
Steralize Prior To Use | true |
Device Is Sterile | false |
[04560224971501]
Moist Heat or Steam Sterilization
[04560224971501]
Moist Heat or Steam Sterilization
[04560224971501]
Moist Heat or Steam Sterilization
[04560224971501]
Moist Heat or Steam Sterilization
[04560224971501]
Moist Heat or Steam Sterilization
[04560224971501]
Moist Heat or Steam Sterilization
[04560224971501]
Moist Heat or Steam Sterilization
[04560224971501]
Moist Heat or Steam Sterilization
[04560224971501]
Moist Heat or Steam Sterilization
[04560224971501]
Moist Heat or Steam Sterilization
[04560224971501]
Moist Heat or Steam Sterilization
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2022-08-11 |
Device Publish Date | 2022-08-03 |
04560264573741 | FC |
04560224971501 | FC |