Klein Touch Pump KTP

GUDID 08169890200142

Klein Touch Pump

HK SURGICAL INC.

General-purpose infusion pump, line-powered General-purpose infusion pump, line-powered General-purpose infusion pump, line-powered General-purpose infusion pump, line-powered General-purpose infusion pump, line-powered General-purpose infusion pump, line-powered General-purpose infusion pump, line-powered General-purpose infusion pump, line-powered General-purpose infusion pump, line-powered General-purpose infusion pump, line-powered General-purpose infusion pump, line-powered General-purpose infusion pump, line-powered General-purpose infusion pump, line-powered General-purpose infusion pump, line-powered Bedside infusion pump Bedside infusion pump Bedside infusion pump Bedside infusion pump Bedside infusion pump Bedside infusion pump Bedside infusion pump Bedside infusion pump Bedside infusion pump Bedside infusion pump Bedside infusion pump, single-channel Bedside infusion pump, single-channel Bedside infusion pump, single-channel Bedside infusion pump, single-channel Bedside infusion pump, single-channel Bedside infusion pump, single-channel Bedside infusion pump, single-channel Bedside infusion pump, single-channel Bedside infusion pump, single-channel Bedside infusion pump, single-channel Bedside infusion pump, single-channel Bedside infusion pump, single-channel Bedside infusion pump, single-channel Bedside infusion pump, single-channel Bedside infusion pump, single-channel Bedside infusion pump, single-channel
Primary Device ID08169890200142
NIH Device Record Keybb6fdeaf-24fc-401d-8198-f4dcd4f3990c
Commercial Distribution Discontinuation2020-08-10
Commercial Distribution StatusNot in Commercial Distribution
Brand NameKlein Touch Pump
Version Model NumberKTP
Catalog NumberKTP
Company DUNS106885259
Company NameHK SURGICAL 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 Perscriptionfalse
OTC Over-The-Counterfalse

Customer Support Contacts

Phone949-369-0101
Emailhkinfo@hksurgical.com
Phone949-369-0101
Emailhkinfo@hksurgical.com
Phone949-369-0101
Emailhkinfo@hksurgical.com
Phone949-369-0101
Emailhkinfo@hksurgical.com
Phone949-369-0101
Emailhkinfo@hksurgical.com
Phone949-369-0101
Emailhkinfo@hksurgical.com
Phone949-369-0101
Emailhkinfo@hksurgical.com
Phone949-369-0101
Emailhkinfo@hksurgical.com
Phone949-369-0101
Emailhkinfo@hksurgical.com
Phone949-369-0101
Emailhkinfo@hksurgical.com
Phone949-369-0101
Emailhkinfo@hksurgical.com
Phone949-369-0101
Emailhkinfo@hksurgical.com
Phone949-369-0101
Emailhkinfo@hksurgical.com
Phone949-369-0101
Emailhkinfo@hksurgical.com
Phone949-369-0101
Emailhkinfo@hksurgical.com
Phone949-369-0101
Emailhkinfo@hksurgical.com
Phone949-369-0101
Emailhkinfo@hksurgical.com
Phone949-369-0101
Emailhkinfo@hksurgical.com
Phone949-369-0101
Emailhkinfo@hksurgical.com
Phone949-369-0101
Emailhkinfo@hksurgical.com
Phone949-369-0101
Emailhkinfo@hksurgical.com
Phone949-369-0101
Emailhkinfo@hksurgical.com
Phone949-369-0101
Emailhkinfo@hksurgical.com
Phone949-369-0101
Emailhkinfo@hksurgical.com
Phone949-369-0101
Emailhkinfo@hksurgical.com
Phone949-369-0101
Emailhkinfo@hksurgical.com
Phone949-369-0101
Emailhkinfo@hksurgical.com
Phone949-369-0101
Emailhkinfo@hksurgical.com
Phone949-369-0101
Emailhkinfo@hksurgical.com
Phone949-369-0101
Emailhkinfo@hksurgical.com
Phone949-369-0101
Emailhkinfo@hksurgical.com
Phone949-369-0101
Emailhkinfo@hksurgical.com
Phone949-369-0101
Emailhkinfo@hksurgical.com
Phone949-369-0101
Emailhkinfo@hksurgical.com
Phone949-369-0101
Emailhkinfo@hksurgical.com
Phone949-369-0101
Emailhkinfo@hksurgical.com
Phone949-369-0101
Emailhkinfo@hksurgical.com
Phone949-369-0101
Emailhkinfo@hksurgical.com
Phone949-369-0101
Emailhkinfo@hksurgical.com
Phone949-369-0101
Emailhkinfo@hksurgical.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100816989020140 [Primary]
GS108169890200142 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

FRNPump, Infusion

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number4
Public Version Date2020-08-11
Device Publish Date2016-09-21

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