Primary Device ID | 00660483163212 |
NIH Device Record Key | 483677fc-bde4-4b0c-999f-de443824c04a |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Detojet |
Version Model Number | 1 Quart bottle |
Catalog Number | 1632-1 |
Company DUNS | 001478726 |
Company Name | ALCONOX INC |
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 | false |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | true |
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 | 00660483163212 [Primary] |
FLG | Cleaner, Ultrasonic, Medical Instrument |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2020-10-05 |
Device Publish Date | 2020-09-27 |
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00660483160112 | Cleaner for ultrasonic cleaning of medical devices |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
DETOJET 87338699 5349122 Live/Registered |
Alconox, Inc. 2017-02-16 |
DETOJET 76624932 3048210 Dead/Cancelled |
ALCONOX, INC. 2004-12-17 |