ServiPlex

GUDID 00810050861977

ASSEMBLY - SYSTEMS – SERVIPLEX

LIFEPORT, LLC

Desk mount
Primary Device ID00810050861977
NIH Device Record Keyb7c5198f-63d0-43b0-817a-b4bfea11c750
Commercial Distribution StatusIn Commercial Distribution
Brand NameServiPlex
Version Model Number0404-0301-01-02
Company DUNS556196210
Company NameLIFEPORT, LLC
Device Count1
DM Exemptfalse
Pre-market Exempttrue
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 Perscriptionfalse
OTC Over-The-Counterfalse

Customer Support Contacts

Phone360-225-1212
EmailCustomerService@lifeport.com
Phone360-225-1212
EmailCustomerService@lifeport.com
Phone360-225-1212
EmailCustomerService@lifeport.com
Phone360-225-1212
EmailCustomerService@lifeport.com
Phone360-225-1212
EmailCustomerService@lifeport.com
Phone360-225-1212
EmailCustomerService@lifeport.com
Phone360-225-1212
EmailCustomerService@lifeport.com
Phone360-225-1212
EmailCustomerService@lifeport.com
Phone360-225-1212
EmailCustomerService@lifeport.com
Phone360-225-1212
EmailCustomerService@lifeport.com
Phone360-225-1212
EmailCustomerService@lifeport.com
Phone360-225-1212
EmailCustomerService@lifeport.com
Phone360-225-1212
EmailCustomerService@lifeport.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100810050861977 [Primary]

FDA Product Code

FOXStand, Infusion

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2022-05-06
Device Publish Date2022-04-28

On-Brand Devices [ServiPlex]

00810050861977ASSEMBLY - SYSTEMS – SERVIPLEX
00810050861960ASSEMBLY - SYSTEMS – SERVIPLEX
00810050862905ASSEMBLY - SERVIPLEX
00810050862912ASSEMBLY - SERVIPLEX

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