GF Glass Fiber Post Kit

GUDID 00852253006328

Root canal post for core build up

J. MORITA U.S.A., INC

Root canal post kit
Primary Device ID00852253006328
NIH Device Record Key0e6f5323-8e1c-4203-b355-76c9eed2f159
Commercial Distribution StatusIn Commercial Distribution
Brand NameGF Glass Fiber Post Kit
Version Model Number23100580
Company DUNS021866033
Company NameJ. MORITA U.S.A., INC
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kittrue
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone9494651051
Emailtinoue@jmoritausa.com
Phone9494651051
Emailtinoue@jmoritausa.com
Phone9494651051
Emailtinoue@jmoritausa.com
Phone9494651051
Emailtinoue@jmoritausa.com
Phone9494651051
Emailtinoue@jmoritausa.com
Phone9494651051
Emailtinoue@jmoritausa.com
Phone9494651051
Emailtinoue@jmoritausa.com
Phone9494651051
Emailtinoue@jmoritausa.com
Phone9494651051
Emailtinoue@jmoritausa.com
Phone9494651051
Emailtinoue@jmoritausa.com
Phone9494651051
Emailtinoue@jmoritausa.com
Phone9494651051
Emailtinoue@jmoritausa.com
Phone9494651051
Emailtinoue@jmoritausa.com
Phone9494651051
Emailtinoue@jmoritausa.com
Phone9494651051
Emailtinoue@jmoritausa.com
Phone9494651051
Emailtinoue@jmoritausa.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100852253006328 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

ELRPost, Root Canal

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2021-11-05
Device Publish Date2021-10-28

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