UF(II) Eco Transfer Impression Coping

GUDID 08800049432464

DIO Corporation

Dental implant suprastructure, temporary, preformed, single-use Dental implant suprastructure, temporary, preformed, single-use Dental implant suprastructure, temporary, preformed, single-use Dental implant suprastructure, temporary, preformed, single-use Dental implant suprastructure, temporary, preformed, single-use Dental implant suprastructure, temporary, preformed, single-use Dental implant suprastructure, temporary, preformed, single-use Dental implant suprastructure, temporary, preformed, single-use Dental implant suprastructure, temporary, preformed, single-use Dental implant suprastructure, temporary, preformed, single-use Dental implant suprastructure, temporary, preformed, single-use Dental implant suprastructure, temporary, preformed, single-use Dental implant suprastructure, temporary, preformed, single-use Dental implant suprastructure, temporary, preformed, single-use Dental implant suprastructure, temporary, preformed, single-use Dental implant suprastructure, temporary, preformed, single-use Dental implant suprastructure, temporary, preformed, single-use Dental implant suprastructure, temporary, preformed, single-use
Primary Device ID08800049432464
NIH Device Record Keyce0d7109-e690-4d97-846f-07e5e5484925
Commercial Distribution StatusIn Commercial Distribution
Brand NameUF(II) Eco Transfer Impression Coping
Version Model NumberUSTI 5510H
Company DUNS631085206
Company NameDIO Corporation
Device Count1
DM Exempttrue
Pre-market Exempttrue
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 Perscriptiontrue
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS108800049432464 [Primary]

FDA Product Code

NDPAccessories, Implant, Dental, Endosseous

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[08800049432464]

Moist Heat or Steam Sterilization


[08800049432464]

Moist Heat or Steam Sterilization


[08800049432464]

Moist Heat or Steam Sterilization


[08800049432464]

Moist Heat or Steam Sterilization


[08800049432464]

Moist Heat or Steam Sterilization


[08800049432464]

Moist Heat or Steam Sterilization


[08800049432464]

Moist Heat or Steam Sterilization


[08800049432464]

Moist Heat or Steam Sterilization


[08800049432464]

Moist Heat or Steam Sterilization


[08800049432464]

Moist Heat or Steam Sterilization


[08800049432464]

Moist Heat or Steam Sterilization


[08800049432464]

Moist Heat or Steam Sterilization


[08800049432464]

Moist Heat or Steam Sterilization


[08800049432464]

Moist Heat or Steam Sterilization


[08800049432464]

Moist Heat or Steam Sterilization


[08800049432464]

Moist Heat or Steam Sterilization


[08800049432464]

Moist Heat or Steam Sterilization


[08800049432464]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2023-09-11
Device Publish Date2023-09-01

On-Brand Devices [UF(II) Eco Transfer Impression Coping]

08800049442999USTI 4510N
08800049442982USTI 4510H
08800049436448USNTI 4210N
08800049436424USNTI 4210H
08800049432495USTI 6510N
08800049432488USTI 6510H
08800049432471USTI 5510N
08800049432464USTI 5510H
08800049432457USTI 4810N
08800049432440USTI 4810H
08800049431818USNTI 4010N
08800049431801USNTI 4010H

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