Reverse Driver

GUDID 08809917144737

Osstem Implant Co., Ltd.

Surgical screwdriver, single-use
Primary Device ID08809917144737
NIH Device Record Key2cf4516e-92e1-485a-8fad-4371e129589b
Commercial Distribution StatusIn Commercial Distribution
Brand NameReverse Driver
Version Model NumberORVDRS
Company DUNS689051793
Company NameOsstem Implant Co., Ltd.
Device Count1
DM Exemptfalse
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 Numbertrue
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
GS108809917144737 [Primary]

FDA Product Code

NDPAccessories, Implant, Dental, Endosseous

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[08809917144737]

Moist Heat or Steam Sterilization


[08809917144737]

Moist Heat or Steam Sterilization


[08809917144737]

Moist Heat or Steam Sterilization


[08809917144737]

Moist Heat or Steam Sterilization


[08809917144737]

Moist Heat or Steam Sterilization


[08809917144737]

Moist Heat or Steam Sterilization


[08809917144737]

Moist Heat or Steam Sterilization


[08809917144737]

Moist Heat or Steam Sterilization


[08809917144737]

Moist Heat or Steam Sterilization


[08809917144737]

Moist Heat or Steam Sterilization


[08809917144737]

Moist Heat or Steam Sterilization


[08809917144737]

Moist Heat or Steam Sterilization


[08809917144737]

Moist Heat or Steam Sterilization


Device Entry Metadata

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

On-Brand Devices [Reverse Driver]

08809917144737ORVDRS
08809917144720ORVDRL
08809917144713ORVDML
08809917144812HRVDRS
08809917144805HRVDRL
08809917144799HRVDML

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