BluPRO® TL-220T-A1

GUDID 04931921019696

Multi-site probe Adults, child (3 kg or more)

NIHON KOHDEN AMERICA, INC.

Pulse oximeter probe, reusable
Primary Device ID04931921019696
NIH Device Record Key488303fc-f914-43be-bb1d-91917e1da722
Commercial Distribution StatusIn Commercial Distribution
Brand NameBluPRO®
Version Model NumberTL-220T
Catalog NumberTL-220T-A1
Company DUNS021063219
Company NameNIHON KOHDEN AMERICA, 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 Datetrue
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(800)325-0283
Emailinfo@nkusa.com
Phone+1(800)325-0283
Emailinfo@nkusa.com
Phone+1(800)325-0283
Emailinfo@nkusa.com
Phone+1(800)325-0283
Emailinfo@nkusa.com
Phone+1(800)325-0283
Emailinfo@nkusa.com
Phone+1(800)325-0283
Emailinfo@nkusa.com
Phone+1(800)325-0283
Emailinfo@nkusa.com
Phone+1(800)325-0283
Emailinfo@nkusa.com
Phone+1(800)325-0283
Emailinfo@nkusa.com
Phone+1(800)325-0283
Emailinfo@nkusa.com
Phone+1(800)325-0283
Emailinfo@nkusa.com
Phone+1(800)325-0283
Emailinfo@nkusa.com
Phone+1(800)325-0283
Emailinfo@nkusa.com
Phone+1(800)325-0283
Emailinfo@nkusa.com
Phone+1(800)325-0283
Emailinfo@nkusa.com
Phone+1(800)325-0283
Emailinfo@nkusa.com
Phone+1(800)325-0283
Emailinfo@nkusa.com
Phone+1(800)325-0283
Emailinfo@nkusa.com
Phone+1(800)325-0283
Emailinfo@nkusa.com
Phone+1(800)325-0283
Emailinfo@nkusa.com
Phone+1(800)325-0283
Emailinfo@nkusa.com
Phone+1(800)325-0283
Emailinfo@nkusa.com
Phone+1(800)325-0283
Emailinfo@nkusa.com
Phone+1(800)325-0283
Emailinfo@nkusa.com
Phone+1(800)325-0283
Emailinfo@nkusa.com
Phone+1(800)325-0283
Emailinfo@nkusa.com
Phone+1(800)325-0283
Emailinfo@nkusa.com
Phone+1(800)325-0283
Emailinfo@nkusa.com
Phone+1(800)325-0283
Emailinfo@nkusa.com
Phone+1(800)325-0283
Emailinfo@nkusa.com
Phone+1(800)325-0283
Emailinfo@nkusa.com

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Device Identifiers

Device Issuing AgencyDevice ID
GS104931921019696 [Primary]

FDA Product Code

GWFStimulator, Electrical, Evoked Response

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2021-06-24
Device Publish Date2021-06-16

On-Brand Devices [BluPRO®]

00841983102752Finger probe Adult, child (20 kg or more) Finger or toe
00841983102691Multi-site probe Adults, child (3 kg or more)
00841983102684Finger probe Adult, child (20kg or more) Finger
04931921019696Multi-site probe Adults, child (3 kg or more)
10841983102742SpO2 probe Child / Infant (from 3 to 20 kg) Finger or toe, disposable
10841983102735SpO2 probe Adults (40 kg or more) Finger or toe, disposable
10841983102728SpO2 probe Child (from 10 to 50 kg) Finger or toe, disposable
10841983102711SpO2 probe Adults (30 kg or more) Finger or toe, disposable, 160cm cable
10841983102704SpO2 probe Adults (30 kg or more) Finger or toe, disposable, 80cm cable

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