Primary Device ID | 00818365020041 |
NIH Device Record Key | cc619787-4619-4d3d-94a5-d6a3b73e1342 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | EdgeEndo Chlohexidine |
Version Model Number | EECHX |
Company DUNS | 078474365 |
Company Name | EDGE ENDO 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 | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Total Volume | 480 Milliliter |
Total Volume | 480 Milliliter |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00818365020041 [Primary] |
KJJ | Cleanser, Root Canal |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-10-05 |
Device Publish Date | 2017-09-28 |
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