DIO Screw Guide Tap

GUDID 08800049204016

DIO Corporation

Dental prosthesis removal instrument
Primary Device ID08800049204016
NIH Device Record Key7b2f4bb6-eb1e-494b-9aaa-5437dd2abbed
Commercial Distribution StatusIn Commercial Distribution
Brand NameDIO Screw Guide Tap
Version Model NumberSGT 1618A
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 Usefalse
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
GS108800049204016 [Primary]

FDA Product Code

DZNInstruments, Dental Hand

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[08800049204016]

Moist Heat or Steam Sterilization


[08800049204016]

Moist Heat or Steam Sterilization


[08800049204016]

Moist Heat or Steam Sterilization


[08800049204016]

Moist Heat or Steam Sterilization


[08800049204016]

Moist Heat or Steam Sterilization


[08800049204016]

Moist Heat or Steam Sterilization


[08800049204016]

Moist Heat or Steam Sterilization


[08800049204016]

Moist Heat or Steam Sterilization


[08800049204016]

Moist Heat or Steam Sterilization


[08800049204016]

Moist Heat or Steam Sterilization


[08800049204016]

Moist Heat or Steam Sterilization


[08800049204016]

Moist Heat or Steam Sterilization


[08800049204016]

Moist Heat or Steam Sterilization


[08800049204016]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2025-04-18
Device Publish Date2022-12-08

On-Brand Devices [DIO Screw Guide Tap]

08800049204092SGT 2518A
08800049204061SGT 2018A
08800049204016SGT 1618A
08800049204009SGT 1418A

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