No-Mount Driver

GUDID 08800011260293

Point Nix Co., Ltd.

Surgical screwdriver, reusable Surgical screwdriver, reusable Surgical screwdriver, reusable Surgical screwdriver, reusable Surgical screwdriver, reusable Surgical screwdriver, reusable Surgical screwdriver, reusable Surgical screwdriver, reusable Surgical screwdriver, reusable Surgical screwdriver, reusable Surgical screwdriver, reusable Surgical screwdriver, reusable Surgical screwdriver, reusable Surgical screwdriver, reusable Surgical screwdriver, reusable Surgical screwdriver, reusable Surgical screwdriver, reusable Surgical screwdriver, reusable Surgical screwdriver, reusable Surgical screwdriver, reusable Surgical screwdriver, reusable Surgical screwdriver, reusable Surgical screwdriver, reusable Surgical screwdriver, reusable Surgical screwdriver, reusable Surgical screwdriver, reusable Surgical screwdriver, reusable Surgical screwdriver, reusable Surgical screwdriver, reusable Surgical screwdriver, reusable Surgical screwdriver, reusable Surgical screwdriver, reusable Surgical screwdriver, reusable Surgical screwdriver, reusable
Primary Device ID08800011260293
NIH Device Record Key10e4da2c-8c05-428f-bb75-bda7af0ed3b4
Commercial Distribution StatusIn Commercial Distribution
Brand NameNo-Mount Driver
Version Model NumberOFDM2100
Company DUNS695333960
Company NamePoint Nix 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 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
GS108800011260293 [Primary]

FDA Product Code

NDPAccessories, Implant, Dental, Endosseous

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[08800011260293]

Moist Heat or Steam Sterilization


[08800011260293]

Moist Heat or Steam Sterilization


[08800011260293]

Moist Heat or Steam Sterilization


[08800011260293]

Moist Heat or Steam Sterilization


[08800011260293]

Moist Heat or Steam Sterilization


[08800011260293]

Moist Heat or Steam Sterilization


[08800011260293]

Moist Heat or Steam Sterilization


[08800011260293]

Moist Heat or Steam Sterilization


[08800011260293]

Moist Heat or Steam Sterilization


[08800011260293]

Moist Heat or Steam Sterilization


[08800011260293]

Moist Heat or Steam Sterilization


[08800011260293]

Moist Heat or Steam Sterilization


[08800011260293]

Moist Heat or Steam Sterilization


[08800011260293]

Moist Heat or Steam Sterilization


[08800011260293]

Moist Heat or Steam Sterilization


[08800011260293]

Moist Heat or Steam Sterilization


[08800011260293]

Moist Heat or Steam Sterilization


[08800011260293]

Moist Heat or Steam Sterilization


[08800011260293]

Moist Heat or Steam Sterilization


[08800011260293]

Moist Heat or Steam Sterilization


[08800011260293]

Moist Heat or Steam Sterilization


[08800011260293]

Moist Heat or Steam Sterilization


[08800011260293]

Moist Heat or Steam Sterilization


[08800011260293]

Moist Heat or Steam Sterilization


[08800011260293]

Moist Heat or Steam Sterilization


[08800011260293]

Moist Heat or Steam Sterilization


[08800011260293]

Moist Heat or Steam Sterilization


[08800011260293]

Moist Heat or Steam Sterilization


[08800011260293]

Moist Heat or Steam Sterilization


[08800011260293]

Moist Heat or Steam Sterilization


[08800011260293]

Moist Heat or Steam Sterilization


[08800011260293]

Moist Heat or Steam Sterilization


[08800011260293]

Moist Heat or Steam Sterilization


[08800011260293]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2022-03-01
Device Publish Date2022-02-21

On-Brand Devices [No-Mount Driver]

08800011260309OFDM2500
08800011260293OFDM2100

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