TL-052S

GUDID 10841983102667

SpO2 probe Adults, child (from 15 to 50 kg) Finger, disposable

NIHON KOHDEN AMERICA, INC.

Pulse oximeter probe, single-use
Primary Device ID10841983102667
NIH Device Record Key38d7350e-53d2-4c6a-8e33-c71e1f391ee2
Commercial Distribution StatusIn Commercial Distribution
Version Model NumberTL-052S
Catalog NumberTL-052S
Company DUNS021063219
Company NameNIHON KOHDEN AMERICA, INC.
Device Count5
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
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

Device Dimensions

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Device Size Text, specify0
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Device Identifiers

Device Issuing AgencyDevice ID
GS100841983102660 [Unit of Use]
GS110841983102667 [Primary]

FDA Product Code

DRTMONITOR, CARDIAC (INCL. CARDIOTACHOMETER & RATE ALARM)

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2021-11-10
Device Publish Date2016-09-19

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