Primary Device ID | 03760140703175 |
NIH Device Record Key | e8937b42-2614-4d86-8ab2-976ffa6aacd3 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | SAFETY PLUS KIT 25G LONG |
Version Model Number | 01N4252 |
Company DUNS | 275273795 |
Company Name | SEPTODONT SAS SPECIALITES SEPTODONT |
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 | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | true |
Donation Id Number | true |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | (303) 665-7535 |
usregulatoryaffairs@septodont.com |
Storage Environment Temperature | Between 0 Degrees Celsius and 30 Degrees Celsius |
Device Issuing Agency | Device ID |
---|---|
GS1 | 03760140703175 [Primary] |
EJI | Syringe, Cartridge |
Steralize Prior To Use | true |
Device Is Sterile | true |
[03760140703175]
Dry Heat Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2019-11-15 |
Device Publish Date | 2016-09-12 |
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