Temporary Cylinder MTEM 5412N

GUDID 08800049251423

DIO Corporation

Dental implant suprastructure, permanent, preformed
Primary Device ID08800049251423
NIH Device Record Keye0105c29-090f-4010-9965-147afb62cc90
Commercial Distribution StatusIn Commercial Distribution
Brand NameTemporary Cylinder
Version Model NumberMTEM 5412N
Catalog NumberMTEM 5412N
Company DUNS631085206
Company NameDIO Corporation
Device Count1
DM Exemptfalse
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 Numbertrue
Manufacturing Datetrue
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS108800049251423 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

NHAAbutment, Implant, Dental, Endosseous

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[08800049251423]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2020-03-18
Device Publish Date2020-03-10

On-Brand Devices [Temporary Cylinder]

08800049251423MTEM 5412N
08800049251416MTEM 5412H

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