Primary Device ID | 04560264562370 |
NIH Device Record Key | 1a24c681-5b63-4a90-8a18-40a22bd73645 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | VA-LUX-HP |
Version Model Number | VA-LUX-HP |
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 | 04560264557253 [Direct Marking] |
GS1 | 04560264562370 [Primary] |
ELC | Scaler, ultrasonic |
Steralize Prior To Use | true |
Device Is Sterile | false |
[04560264562370]
Moist Heat or Steam Sterilization
[04560264562370]
Moist Heat or Steam Sterilization
[04560264562370]
Moist Heat or Steam Sterilization
[04560264562370]
Moist Heat or Steam Sterilization
[04560264562370]
Moist Heat or Steam Sterilization
[04560264562370]
Moist Heat or Steam Sterilization
[04560264562370]
Moist Heat or Steam Sterilization
[04560264562370]
Moist Heat or Steam Sterilization
[04560264562370]
Moist Heat or Steam Sterilization
[04560264562370]
Moist Heat or Steam Sterilization
[04560264562370]
Moist Heat or Steam Sterilization
[04560264562370]
Moist Heat or Steam Sterilization
[04560264562370]
Moist Heat or Steam Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2018-08-23 |
Device Publish Date | 2016-09-16 |
04560264562370 | VA-LUX-HP |
04560264560321 | VA-LUX-HP |
04560224972614 | VA-LUX-HP |