NE233 Charger

GUDID 04560264574120

NAKANISHI INC.

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Primary Device ID04560264574120
NIH Device Record Key0d540463-5b14-4a93-a8e9-5093299d2b45
Commercial Distribution StatusIn Commercial Distribution
Brand NameNE233 Charger
Version Model NumberNE233 Charger
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
GS104560264574120 [Primary]

FDA Product Code

EKXHandpiece, direct drive, ac-powered

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2020-08-27
Device Publish Date2020-08-19

On-Brand Devices [NE233 Charger]

04560264574120NE233 Charger
04560264510654NE233 Charger

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