Paro® Non-Latex Rubber Dam 838080

GUDID 07540172014571

Dental isolation dam

CLINICIAN'S CHOICE DENTAL PRODUCTS, INC.

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Primary Device ID07540172014571
NIH Device Record Key82a81a8e-3ce5-480f-86f2-771ca497d55b
Commercial Distribution StatusIn Commercial Distribution
Brand NameParo® Non-Latex Rubber Dam
Version Model Number838080
Catalog Number838080
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 Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datetrue
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
Phone+1(800)265-3444
Emailinfo@clinicianschoice.com
Phone+1(800)265-3444
Emailinfo@clinicianschoice.com
Phone+1(800)265-3444
Emailinfo@clinicianschoice.com
Phone+1(800)265-3444
Emailinfo@clinicianschoice.com
Phone+1(800)265-3444
Emailinfo@clinicianschoice.com
Phone+1(800)265-3444
Emailinfo@clinicianschoice.com
Phone+1(800)265-3444
Emailinfo@clinicianschoice.com
Phone+1(800)265-3444
Emailinfo@clinicianschoice.com
Phone+1(800)265-3444
Emailinfo@clinicianschoice.com
Phone+1(800)265-3444
Emailinfo@clinicianschoice.com
Phone+1(800)265-3444
Emailinfo@clinicianschoice.com
Phone+1(800)265-3444
Emailinfo@clinicianschoice.com
Phone+1(800)265-3444
Emailinfo@clinicianschoice.com
Phone+1(800)265-3444
Emailinfo@clinicianschoice.com
Phone+1(800)265-3444
Emailinfo@clinicianschoice.com

Device Dimensions

Device Size Text, specify0
Area/Surface Area36 Square inch
Device Size Text, specify0
Area/Surface Area36 Square inch
Device Size Text, specify0
Area/Surface Area36 Square inch
Device Size Text, specify0
Area/Surface Area36 Square inch
Device Size Text, specify0
Area/Surface Area36 Square inch
Device Size Text, specify0
Area/Surface Area36 Square inch
Device Size Text, specify0
Area/Surface Area36 Square inch
Device Size Text, specify0
Area/Surface Area36 Square inch
Device Size Text, specify0
Area/Surface Area36 Square inch
Device Size Text, specify0
Area/Surface Area36 Square inch
Device Size Text, specify0
Area/Surface Area36 Square inch
Device Size Text, specify0
Area/Surface Area36 Square inch
Device Size Text, specify0
Area/Surface Area36 Square inch
Device Size Text, specify0
Area/Surface Area36 Square inch
Device Size Text, specify0
Area/Surface Area36 Square inch
Device Size Text, specify0

Device Identifiers

Device Issuing AgencyDevice ID
GS107540172014571 [Primary]

FDA Product Code

EIEDAM, RUBBER

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2020-03-25
Device Publish Date2020-03-17