Tower Assembly

GUDID 00810050862394

TOWER ASSEMBLY

LIFEPORT, LLC

Desk mount
Primary Device ID00810050862394
NIH Device Record Key1356b545-2e4b-4598-9978-6f6623acb8cd
Commercial Distribution StatusIn Commercial Distribution
Brand NameTower Assembly
Version Model NumberST2-245-07-A2B1C1D1
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

Phone3602251212
EmailCustomerService@lifeport.com
Phone3602251212
EmailCustomerService@lifeport.com
Phone3602251212
EmailCustomerService@lifeport.com
Phone3602251212
EmailCustomerService@lifeport.com
Phone3602251212
EmailCustomerService@lifeport.com
Phone3602251212
EmailCustomerService@lifeport.com
Phone3602251212
EmailCustomerService@lifeport.com
Phone3602251212
EmailCustomerService@lifeport.com
Phone3602251212
EmailCustomerService@lifeport.com
Phone3602251212
EmailCustomerService@lifeport.com
Phone3602251212
EmailCustomerService@lifeport.com
Phone3602251212
EmailCustomerService@lifeport.com
Phone3602251212
EmailCustomerService@lifeport.com
Phone3602251212
EmailCustomerService@lifeport.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100810050862394 [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 Date2023-04-04
Device Publish Date2023-03-27

On-Brand Devices [Tower Assembly]

00810050860970TOWER ASSEMBLY
00810050861076TOWER ASSEMBLY
00810050862394TOWER ASSEMBLY

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.