UF(II) Eco Pickup Impression Coping

GUDID 08800049431788

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 ID08800049431788
NIH Device Record Key625f2f7d-2bfa-4cda-aadf-1e4ae877e737
Commercial Distribution StatusIn Commercial Distribution
Brand NameUF(II) Eco Pickup Impression Coping
Version Model NumberUSNPI 4006H
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
GS108800049431788 [Primary]

FDA Product Code

NDPAccessories, Implant, Dental, Endosseous

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[08800049431788]

Moist Heat or Steam Sterilization


[08800049431788]

Moist Heat or Steam Sterilization


[08800049431788]

Moist Heat or Steam Sterilization


[08800049431788]

Moist Heat or Steam Sterilization


[08800049431788]

Moist Heat or Steam Sterilization


[08800049431788]

Moist Heat or Steam Sterilization


[08800049431788]

Moist Heat or Steam Sterilization


[08800049431788]

Moist Heat or Steam Sterilization


[08800049431788]

Moist Heat or Steam Sterilization


[08800049431788]

Moist Heat or Steam Sterilization


[08800049431788]

Moist Heat or Steam Sterilization


[08800049431788]

Moist Heat or Steam Sterilization


[08800049431788]

Moist Heat or Steam Sterilization


[08800049431788]

Moist Heat or Steam Sterilization


[08800049431788]

Moist Heat or Steam Sterilization


[08800049431788]

Moist Heat or Steam Sterilization


[08800049431788]

Moist Heat or Steam Sterilization


[08800049431788]

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 Pickup Impression Coping]

08800049442975USPI 4506N
08800049442968USPI 4506H
08800049436387USNPI 4206N
08800049436363USNPI 4206H
08800049432433USPI 6506N
08800049432426USPI 6506H
08800049432419USPI 5506N
08800049432402USPI 5506H
08800049432396USPI 4806N
08800049432389USPI 4806H
08800049431795USNPI 4006N
08800049431788USNPI 4006H

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