Universal Plastic Cylinder Set

GUDID 08800023133745

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 ID08800023133745
NIH Device Record Key5088f0d6-bbaa-4886-910a-ccbe38189d58
Commercial Distribution StatusIn Commercial Distribution
Brand NameUniversal Plastic Cylinder Set
Version Model NumberCUAPCH48S
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
GS108800023133745 [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 Plastic Cylinder Set]

08800023133752CUAPCN48S
08800023133745CUAPCH48S

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