BB-Y

GUDID 04560264572751

NAKANISHI INC.

Dental power tool system handpiece, line-powered Dental power tool system handpiece, line-powered Dental power tool system handpiece, line-powered Dental power tool system handpiece, line-powered Dental power tool system handpiece, line-powered Dental power tool system handpiece, line-powered Dental power tool system handpiece, line-powered Dental power tool system handpiece, line-powered Dental power tool system handpiece, line-powered Dental power tool system handpiece, line-powered Dental power tool system handpiece, line-powered Dental power tool system handpiece, line-powered Dental power tool system handpiece, line-powered Dental power tool system handpiece, line-powered Dental surgical power tool motorized handpiece/set, electric Dental surgical power tool motorized handpiece/set, electric Dental surgical power tool motorized handpiece/set, electric Dental surgical power tool motorized handpiece/set, electric Dental surgical power tool motorized handpiece/set, electric Dental surgical power tool motorized handpiece/set, electric Dental surgical power tool motorized handpiece/set, electric Dental surgical power tool motorized handpiece/set, electric Dental surgical power tool motorized handpiece/set, electric Dental surgical power tool motorized handpiece/set, electric Dental surgical power tool motorized handpiece/set, electric Dental surgical power tool motorized handpiece/set, electric Dental surgical power tool motorized handpiece/set, electric Dental surgical power tool motorized handpiece/set, electric Dental surgical power tool motorized handpiece/set, electric Dental surgical power tool motorized handpiece/set, electric Dental surgical power tool motorized handpiece/set, electric
Primary Device ID04560264572751
NIH Device Record Keye0d7ee9d-511b-4bda-b75e-42e54c78fa35
Commercial Distribution StatusIn Commercial Distribution
Brand NameBB-Y
Version Model NumberBB-Y
Company DUNS690710546
Company NameNAKANISHI INC.
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 Usefalse
Lot Batchfalse
Serial Numbertrue
Manufacturing Datefalse
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
GS104560264572751 [Primary]
GS104589551383009 [Direct Marking]

FDA Product Code

EGSHandpiece, contra- and right-angle attachment, dental

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[04560264572751]

Moist Heat or Steam Sterilization


[04560264572751]

Moist Heat or Steam Sterilization


[04560264572751]

Moist Heat or Steam Sterilization


[04560264572751]

Moist Heat or Steam Sterilization


[04560264572751]

Moist Heat or Steam Sterilization


[04560264572751]

Moist Heat or Steam Sterilization


[04560264572751]

Moist Heat or Steam Sterilization


[04560264572751]

Moist Heat or Steam Sterilization


[04560264572751]

Moist Heat or Steam Sterilization


[04560264572751]

Moist Heat or Steam Sterilization


[04560264572751]

Moist Heat or Steam Sterilization


[04560264572751]

Moist Heat or Steam Sterilization


[04560264572751]

Moist Heat or Steam Sterilization


[04560264572751]

Moist Heat or Steam Sterilization


[04560264572751]

Moist Heat or Steam Sterilization


[04560264572751]

Moist Heat or Steam Sterilization


[04560264572751]

Moist Heat or Steam Sterilization


[04560264572751]

Moist Heat or Steam Sterilization


[04560264572751]

Moist Heat or Steam Sterilization


[04560264572751]

Moist Heat or Steam Sterilization


[04560264572751]

Moist Heat or Steam Sterilization


[04560264572751]

Moist Heat or Steam Sterilization


[04560264572751]

Moist Heat or Steam Sterilization


[04560264572751]

Moist Heat or Steam Sterilization


[04560264572751]

Moist Heat or Steam Sterilization


[04560264572751]

Moist Heat or Steam Sterilization


[04560264572751]

Moist Heat or Steam Sterilization


[04560264572751]

Moist Heat or Steam Sterilization


[04560264572751]

Moist Heat or Steam Sterilization


[04560264572751]

Moist Heat or Steam Sterilization


[04560264572751]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2020-07-17
Device Publish Date2020-07-09

Devices Manufactured by NAKANISHI INC.

04589551363438 - Primado22024-01-24
04560264530225 - Primado22023-11-21
04589551355020 - P300-2A102023-11-21
04589551355037 - P300-2A202023-11-21
04589551355129 - P300-2A402023-11-21
04589551355136 - P300-2A602023-11-21
04589551355228 - P300-2A802023-11-21
04589551355235 - P300-2S102023-11-21

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