Cylinder Screw MSC 1604

GUDID 08800049286586

DIO Corporation

Dental implant suprastructure, permanent, preformed
Primary Device ID08800049286586
NIH Device Record Keyd31e288f-061c-4b9b-83f8-77f53354f122
Commercial Distribution StatusIn Commercial Distribution
Brand NameCylinder Screw
Version Model NumberMSC 1604
Catalog NumberMSC 1604
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
GS108800049286586 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

NHAAbutment, Implant, Dental, Endosseous

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[08800049286586]

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

Devices Manufactured by DIO Corporation

08800049201657 - DIO Open Wrench2023-09-18
08800049302330 - DIO Ratchet Wrench2023-09-18
08800049304129 - DIO Square Wrench2023-09-18
08800049306109 - DIO Torque Wrench2023-09-18
08800049251409 - UF(II) Scan Adapter2023-09-11
08800049430569 - UF(II) Eco Base Abutment2023-09-11
08800049430576 - UF(II) Eco Base Abutment2023-09-11
08800049430583 - UF(II) Eco Base Abutment2023-09-11

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.