UF(II) Eastab Cylinder Semi Final

GUDID 08800049438992

DIO Corporation

Dental implant suprastructure, permanent, preformed
Primary Device ID08800049438992
NIH Device Record Keyd8a09b09-3476-463d-a95b-6e54634a61a9
Commercial Distribution StatusIn Commercial Distribution
Brand NameUF(II) Eastab Cylinder Semi Final
Version Model NumberESMCSF 4806N
Company DUNS631085206
Company NameDIO Corporation
Device Count1
DM Exempttrue
Pre-market Exemptfalse
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 Perscriptionfalse
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS108800049438992 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

NHAAbutment, Implant, Dental, Endosseous

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[08800049438992]

Moist Heat or Steam Sterilization


[08800049438992]

Moist Heat or Steam Sterilization


[08800049438992]

Moist Heat or Steam Sterilization


[08800049438992]

Moist Heat or Steam Sterilization


[08800049438992]

Moist Heat or Steam Sterilization


[08800049438992]

Moist Heat or Steam Sterilization


[08800049438992]

Moist Heat or Steam Sterilization


[08800049438992]

Moist Heat or Steam Sterilization


[08800049438992]

Moist Heat or Steam Sterilization


[08800049438992]

Moist Heat or Steam Sterilization


[08800049438992]

Moist Heat or Steam Sterilization


[08800049438992]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2025-09-26
Device Publish Date2025-09-18

On-Brand Devices [UF(II) Eastab Cylinder Semi Final]

08800049443040ESMCSF 4806H
08800049438992ESMCSF 4806N

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