LOW SPEED AIR MOTOR/HP

GUDID 04560264533752

NAKANISHI INC.

Dental surgical power tool motor, pneumatic Dental surgical power tool motor, pneumatic Dental surgical power tool motor, pneumatic Dental surgical power tool motor, pneumatic Dental surgical power tool motor, pneumatic Dental surgical power tool motor, pneumatic Dental surgical power tool motor, pneumatic Dental surgical power tool motor, pneumatic Dental surgical power tool motor, pneumatic Dental surgical power tool motor, pneumatic Dental surgical power tool motor, pneumatic Dental surgical power tool motorized handpiece/set, pneumatic Dental surgical power tool motorized handpiece/set, pneumatic Dental surgical power tool motorized handpiece/set, pneumatic Dental surgical power tool motorized handpiece/set, pneumatic Dental surgical power tool motorized handpiece/set, pneumatic Dental surgical power tool motorized handpiece/set, pneumatic Dental surgical power tool motorized handpiece/set, pneumatic Dental surgical power tool motorized handpiece/set, pneumatic Dental surgical power tool motorized handpiece/set, pneumatic Dental surgical power tool motorized handpiece/set, pneumatic Dental surgical power tool motorized handpiece/set, pneumatic Dental surgical power tool motorized handpiece/set, pneumatic Dental surgical power tool motorized handpiece/set, pneumatic Dental surgical power tool motorized handpiece/set, pneumatic Dental surgical power tool motorized handpiece/set, pneumatic Dental surgical power tool motorized handpiece/set, pneumatic Dental surgical power tool motorized handpiece/set, pneumatic
Primary Device ID04560264533752
NIH Device Record Keyf14fc520-94df-469f-a5be-d374e07e8396
Commercial Distribution StatusIn Commercial Distribution
Brand NameLOW SPEED AIR MOTOR/HP
Version Model NumberiProphy Air
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
GS104560264533752 [Primary]
GS104589551383351 [Direct Marking]

FDA Product Code

EFBHandpiece, air-powered, dental

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[04560264533752]

Moist Heat or Steam Sterilization


[04560264533752]

Moist Heat or Steam Sterilization


[04560264533752]

Moist Heat or Steam Sterilization


[04560264533752]

Moist Heat or Steam Sterilization


[04560264533752]

Moist Heat or Steam Sterilization


[04560264533752]

Moist Heat or Steam Sterilization


[04560264533752]

Moist Heat or Steam Sterilization


[04560264533752]

Moist Heat or Steam Sterilization


[04560264533752]

Moist Heat or Steam Sterilization


[04560264533752]

Moist Heat or Steam Sterilization


[04560264533752]

Moist Heat or Steam Sterilization


[04560264533752]

Moist Heat or Steam Sterilization


[04560264533752]

Moist Heat or Steam Sterilization


[04560264533752]

Moist Heat or Steam Sterilization


[04560264533752]

Moist Heat or Steam Sterilization


[04560264533752]

Moist Heat or Steam Sterilization


[04560264533752]

Moist Heat or Steam Sterilization


[04560264533752]

Moist Heat or Steam Sterilization


[04560264533752]

Moist Heat or Steam Sterilization


[04560264533752]

Moist Heat or Steam Sterilization


[04560264533752]

Moist Heat or Steam Sterilization


[04560264533752]

Moist Heat or Steam Sterilization


[04560264533752]

Moist Heat or Steam Sterilization


[04560264533752]

Moist Heat or Steam Sterilization


[04560264533752]

Moist Heat or Steam Sterilization


[04560264533752]

Moist Heat or Steam Sterilization


[04560264533752]

Moist Heat or Steam Sterilization


[04560264533752]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2022-11-28
Device Publish Date2020-06-17

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04560264511705 - Primado22024-04-03
04560264511736 - Primado22024-04-03
04560264523081 - Primado22024-04-03
04560264523098 - Primado22024-04-03

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