Primary Device ID | 00303620000048 |
NIH Device Record Key | 58eae33b-6eb9-4351-b366-6a7acfc4a46f |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | SEPTODONT PETITE - BLUE |
Version Model Number | 01N2100 |
Catalog Number | 01N2100 |
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 | false |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | true |
Expiration Date | false |
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 | 00303620000048 [Primary] |
EJI | Syringe, Cartridge |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00303620000048]
Dry Heat Sterilization
[00303620000048]
Dry Heat Sterilization
[00303620000048]
Dry Heat Sterilization
[00303620000048]
Dry Heat Sterilization
[00303620000048]
Dry Heat Sterilization
[00303620000048]
Dry Heat Sterilization
[00303620000048]
Dry Heat Sterilization
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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