Cement Abutment

GUDID 08800023146141

Cybermed Inc.

Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed
Primary Device ID08800023146141
NIH Device Record Key4faa9a33-b3d9-4678-a6f9-103afdb020a4
Commercial Distribution StatusIn Commercial Distribution
Brand NameCement Abutment
Version Model NumberICCAHM4073ES
Company DUNS688248447
Company NameCybermed Inc.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Producttrue
Single Usetrue
Lot Batchtrue
Serial Numbertrue
Manufacturing Datetrue
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latextrue
RX Perscriptionfalse
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+827051187131
Emailkshwan95@cybermed.co.kr
Phone+827051187131
Emailkshwan95@cybermed.co.kr
Phone+827051187131
Emailkshwan95@cybermed.co.kr
Phone+827051187131
Emailkshwan95@cybermed.co.kr
Phone+827051187131
Emailkshwan95@cybermed.co.kr
Phone+827051187131
Emailkshwan95@cybermed.co.kr
Phone+827051187131
Emailkshwan95@cybermed.co.kr

Device Identifiers

Device Issuing AgencyDevice ID
GS108800023146141 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

NHAAbutment, Implant, Dental, Endosseous

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2022-11-10
Device Publish Date2022-11-02

On-Brand Devices [Cement Abutment]

08800023109214CCAHR6072E
08800023109207CCAHR6043E
08800023109191CCAHR6063E
08800023109184CCAHR6073E
08800023109177CCAHR6044E
08800023109160CCAHR6064E
08800023109153CCAHR6074E
08800023109146CCAHR6045E
08800023109139CCAHR6065E
08800023109122CCAHR6075E
08800023109115CCAHR5041E
08800023109108CCAHR5061E
08800023109092CCAHR5071E
08800023109085CCAHR5042E
08800023109078CCAHR5062E
08800023109061CCAHR5072E
08800023109054CCAHR5043E
08800023109047CCAHR5063E
08800023109030CCAHR5073E
08800023109023CCAHR5044E
08800023109016CCAHR5064E
08800023109009CCAHR5074E
08800023108996CCAHR5045E
08800023108989CCAHR5065E
08800023108972CCAHR5075E
08800023108965CCAHR4541E
08800023108958CCAHR4561E
08800023108941CCAHR4571E
08800023108934CCAHR4542E
08800023108927CCAHR4562E
08800023108910CCAHR4572E
08800023108903CCAHR4543E
08800023108897CCAHR4563E
08800023108880CCAHR4573E
08800023108873CCAHR4544E
08800023108866CCAHR4564E
08800023108859CCAHR4574E
08800023108842CCAHR4545E
08800023108835CCAHR4565E
08800023108828CCAHR4575E
08800023108811CCAHR4041E
08800023108804CCAHR4061E
08800023108798CCAHR4071E
08800023108781CCAHR4042E
08800023108774CCAHR4062E
08800023108767CCAHR4072E
08800023108750CCAHR4043E
08800023108743CCAHR4063E
08800023108736CCAHR4073E
08800023108729CCAHR4044E

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