Solid Abutment Set

GUDID 08800023134551

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 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 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 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 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 ID08800023134551
NIH Device Record Key1a6bbfa4-9339-4968-aef1-eec727f5fe05
Commercial Distribution StatusIn Commercial Distribution
Brand NameSolid Abutment Set
Version Model NumberCSAR6074P
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
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
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
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
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
GS108800023134551 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

NHAAbutment, Implant, Dental, Endosseous

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2022-03-07
Device Publish Date2022-02-25

On-Brand Devices [Solid Abutment Set]

08800023134667CSAR6041P
08800023134650CSAR6061P
08800023134643CSAR6071P
08800023134636CSAR6042P
08800023134629CSAR6062P
08800023134612CSAR6072P
08800023134605CSAR6043P
08800023134599CSAR6063P
08800023134582CSAR6073P
08800023134575CSAR6044P
08800023134568CSAR6064P
08800023134551CSAR6074P
08800023134544CSAR6045P
08800023134537CSAR6065P
08800023134520CSAR6075P
08800023134513CSAR5041P
08800023134506CSAR5061P
08800023134490CSAR5071P
08800023134483CSAR5042P
08800023134476CSAR5062P
08800023134469CSAR5072P
08800023134452CSAR5043P
08800023134445CSAR5063P
08800023134438CSAR5073P
08800023134421CSAR5044P
08800023134414CSAR5064P
08800023134407CSAR5074P
08800023134391CSAR5045P
08800023134384CSAR5065P
08800023134377CSAR5075P
08800023134360CSAR4541P
08800023134353CSAR4561P
08800023134346CSAR4571P
08800023134339CSAR4542P
08800023134322CSAR4562P
08800023134315CSAR4572P
08800023134308CSAR4543P
08800023134292CSAR4563P
08800023134285CSAR4573P
08800023134278CSAR4544P
08800023134261CSAR4564P
08800023134254CSAR4574P
08800023134247CSAR4545P
08800023134230CSAR4565P
08800023134223CSAR4575P
08800023134216CSAR4041P
08800023134209CSAR4061P
08800023134193CSAR4071P
08800023134186CSAR4042P
08800023134179CSAR4062P

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