Side Arch

GUDID 00810050861380

INSTALLATION, SIDE ARCH, PIAGGIO P180

LIFEPORT, LLC

Desk mount
Primary Device ID00810050861380
NIH Device Record Keyd7654d32-b805-418b-86b7-3f4f1b3a792c
Commercial Distribution StatusIn Commercial Distribution
Brand NameSide Arch
Version Model Number100-4279-CF2-03
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
Phone360-225-1212
EmailCustomerService@lifeport.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100810050861380 [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 Date2021-07-09
Device Publish Date2021-07-01

On-Brand Devices [Side Arch]

00810050861380INSTALLATION, SIDE ARCH, PIAGGIO P180
00810050862653INSTALLATION - SIDE ARCH

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