FenderWedge 602801

GUDID 17310236028014

Directa AB

Dental wedge, single-use
Primary Device ID17310236028014
NIH Device Record Key7e632e69-6410-4dc7-9e0b-f2589bbeed75
Commercial Distribution StatusIn Commercial Distribution
Brand NameFenderWedge
Version Model NumberValue Pack
Catalog Number602801
Company DUNS353954381
Company NameDirecta AB
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 Batchtrue
Serial Numberfalse
Manufacturing Datetrue
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
GS117310236028014 [Primary]

FDA Product Code

EJBHandle, Instrument, Dental

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2022-12-15
Device Publish Date2022-12-07

On-Brand Devices [FenderWedge ]

17310236027369NG Orange
17310236027352NG Purple
17310236028113Prep Value Pack
17310236028038Value Pack
17310236028021Value Pack
17310236028014Value Pack
17310236028007Value Pack
17310236027543X-small
17310236027536Large
17310236027529Medium
17310236027512Small
17310236027505Assortment
17310236027499Prep

Trademark Results [FenderWedge]

Mark Image

Registration | Serial
Company
Trademark
Application Date
FENDERWEDGE
FENDERWEDGE
79027123 3312815 Live/Registered
Directa AB
2006-01-25

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