FlexiDisc Mini 1/2 Coarse

GUDID D77940221213

COSMEDENT, INC.

Dental abrasive disk, single-use Dental abrasive disk, single-use
Primary Device IDD77940221213
NIH Device Record Key80959a57-1be7-44df-8f69-c420669dc916
Commercial Distribution StatusIn Commercial Distribution
Brand NameFlexiDisc Mini 1/2 Coarse
Version Model Number402212
Company DUNS113911689
Company NameCOSMEDENT, INC.
Device Count1
DM Exemptfalse
Pre-market Exempttrue
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchfalse
Serial Numberfalse
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
HIBCCD77940221213 [Primary]

FDA Product Code

EHJDisk, Abrasive

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2020-05-06
Device Publish Date2020-01-22

On-Brand Devices [FlexiDisc Mini 1/2 Coarse]

D77940221213402212
D77940211212402112

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.