Round bar with rider 05000679

GUDID 07640166515111

Round bar with rider Female part E L50

Cendres+Métaux SA

Bar dental precision attachment
Primary Device ID07640166515111
NIH Device Record Keyb47a894a-6253-4559-a609-8eb432dc20c8
Commercial Distribution StatusIn Commercial Distribution
Brand NameRound bar with rider
Version Model Number05000679
Catalog Number05000679
Company DUNS487506230
Company NameCendres+Métaux SA
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

Customer Support Contacts

Phone+41583602000
Emailinfo@cmsa.ch
Phone+41583602000
Emailinfo@cmsa.ch
Phone+41583602000
Emailinfo@cmsa.ch
Phone+41583602000
Emailinfo@cmsa.ch
Phone+41583602000
Emailinfo@cmsa.ch
Phone+41583602000
Emailinfo@cmsa.ch
Phone+41583602000
Emailinfo@cmsa.ch
Phone+41583602000
Emailinfo@cmsa.ch
Phone+41583602000
Emailinfo@cmsa.ch
Phone+41583602000
Emailinfo@cmsa.ch
Phone+41583602000
Emailinfo@cmsa.ch
Phone+41583602000
Emailinfo@cmsa.ch
Phone+41583602000
Emailinfo@cmsa.ch
Phone+41583602000
Emailinfo@cmsa.ch

Device Identifiers

Device Issuing AgencyDevice ID
GS107640166515111 [Primary]

FDA Product Code

EGGAttachment, Precision, All

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2020-08-11
Device Publish Date2020-08-03

On-Brand Devices [Round bar with rider]

07640166515111Round bar with rider Female part E L50
07640166514831Round bar with rider Transfer jig
07640166513797Round bar with rider Female part E
07640239931602Round bar with rider Female part E

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