Primary Device ID | 00303620000758 |
NIH Device Record Key | cb81ea92-a9db-465e-8a52-e45fba44a4b1 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | SEPTODONT SAMPLER 5-A2 COMPULES |
Version Model Number | 01C2059 |
Company DUNS | 012925513 |
Company Name | SEPTODONT, 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 | true |
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 |
Phone | (303) 665-7535 |
usregulatoryaffairs@septodont.com |
Weight | 0.3 Gram |
Storage Environment Temperature | Between 15 Degrees Celsius and 24 Degrees Celsius |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00303620000758 [Primary] |
EBF | Material, Tooth Shade, Resin |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2018-03-29 |
Device Publish Date | 2016-09-12 |
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