Universal Abutment Set

GUDID 08800023133431

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 ID08800023133431
NIH Device Record Key704b7966-2ee7-4ea0-9d81-f0a551ea3d19
Commercial Distribution StatusIn Commercial Distribution
Brand NameUniversal Abutment Set
Version Model NumberCUASM4804C
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
GS108800023133431 [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 [Universal Abutment Set]

08800023133493CUASR4802C
08800023133486CUASR4803C
08800023133479CUASR4804C
08800023133462CUASR4805C
08800023133455CUASM4802C
08800023133448CUASM4803C
08800023133431CUASM4804C
08800023133424CUASM4805C

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