SEPTODONT FUSION(TITANIUM) SYRINGE

GUDID 00303620000055

Aspirating Syringe Medium Titanium Fusion Septodont USA

SEPTODONT, INC

Syringe-loaded injector, manual, professional
Primary Device ID00303620000055
NIH Device Record Key63102879-6247-465c-87f9-b19197951453
Commercial Distribution StatusIn Commercial Distribution
Brand NameSEPTODONT FUSION(TITANIUM) SYRINGE
Version Model Number01N2105
Company DUNS012925513
Company NameSEPTODONT, INC
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchtrue
Serial Numberfalse
Manufacturing Datetrue
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS100303620000055 [Primary]

FDA Product Code

EJISyringe, Cartridge

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00303620000055]

Dry Heat Sterilization


[00303620000055]

Dry Heat Sterilization


[00303620000055]

Dry Heat Sterilization


[00303620000055]

Dry Heat Sterilization


[00303620000055]

Dry Heat Sterilization


[00303620000055]

Dry Heat Sterilization


[00303620000055]

Dry Heat Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2018-03-29
Device Publish Date2016-09-12

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