NLX

GUDID 04560264521193

NAKANISHI INC.

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Primary Device ID04560264521193
NIH Device Record Keyf1aefe7d-6eef-4106-b9ed-6fbeeca43c62
Commercial Distribution Discontinuation2022-09-23
Commercial Distribution StatusIn Commercial Distribution
Brand NameNLX
Version Model NumberNLX nano
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
GS104560264521193 [Primary]

FDA Product Code

EBWController, foot, handpiece and cord

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[04560264521193]

Moist Heat or Steam Sterilization


[04560264521193]

Moist Heat or Steam Sterilization


[04560264521193]

Moist Heat or Steam Sterilization


[04560264521193]

Moist Heat or Steam Sterilization


[04560264521193]

Moist Heat or Steam Sterilization


[04560264521193]

Moist Heat or Steam Sterilization


[04560264521193]

Moist Heat or Steam Sterilization


[04560264521193]

Moist Heat or Steam Sterilization


[04560264521193]

Moist Heat or Steam Sterilization


[04560264521193]

Moist Heat or Steam Sterilization


[04560264521193]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2022-08-11
Device Publish Date2022-08-03

On-Brand Devices [NLX]

04560264522237NLX nano U
04560264521193NLX nano
04560264573628NLX nano U
04560264573307NLX nano S120
04560264572836NLX CDE
04560264572829NLX CD
04560264572812NLX nano
04560264534568NLX nano S120E
04560264523104NLX plus

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