Dual-Force™ Sectional Matrix System Pre-Molar Rings Orange 209007

GUDID 07540172016568

Device to engage the matrices and separate teeth

CLINICIAN'S CHOICE DENTAL PRODUCTS, INC.

Dental matrix band retainer
Primary Device ID07540172016568
NIH Device Record Key3e6f00f5-b2c2-426e-a7cc-63478062866f
Commercial Distribution StatusIn Commercial Distribution
Brand NameDual-Force™ Sectional Matrix System Pre-Molar Rings Orange
Version Model Number209007
Catalog Number209007
Company DUNS626406016
Company NameCLINICIAN'S CHOICE DENTAL PRODUCTS, INC.
Device Count1
DM Exempttrue
Pre-market Exempttrue
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchfalse
Serial Numberfalse
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(800)265-3444
Emailinfo@clinicianschoice.com

Device Identifiers

Device Issuing AgencyDevice ID
GS107540172016568 [Primary]

FDA Product Code

DZNINSTRUMENTS, DENTAL HAND

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2020-03-27
Device Publish Date2020-03-19