Implant Forcep System 067300

GUDID 07540172012867

Dental implant/prosthesis surgical procedure kit

CLINICIAN'S CHOICE DENTAL PRODUCTS, INC.

Dental implant/prosthesis handling forceps
Primary Device ID07540172012867
NIH Device Record Keycdf2b409-1e6f-4c57-a1db-661f54861487
Commercial Distribution StatusIn Commercial Distribution
Brand NameImplant Forcep System
Version Model Number067300
Catalog Number067300
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
Email[email protected]

Device Identifiers

Device Issuing AgencyDevice ID
GS107540172012867 [Primary]

FDA Product Code

EJGFORCEPS, RUBBER DAM CLAMP

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