FloPatch

GUDID 20627987360114

1929803 Ontario Corp

Noninvasive vascular ultrasound system probe Noninvasive vascular ultrasound system probe Noninvasive vascular ultrasound system probe Noninvasive vascular ultrasound system probe Noninvasive vascular ultrasound system probe Noninvasive vascular ultrasound system probe Noninvasive vascular ultrasound system probe Noninvasive vascular ultrasound system probe Noninvasive vascular ultrasound system probe Noninvasive vascular ultrasound system probe Noninvasive vascular ultrasound system probe Noninvasive vascular ultrasound system probe Noninvasive vascular ultrasound system probe Noninvasive vascular ultrasound system probe
Primary Device ID20627987360114
NIH Device Record Keye5f756c4-4531-41aa-9ad2-5381a91410b6
Commercial Distribution StatusIn Commercial Distribution
Brand NameFloPatch
Version Model NumberFP120
Company DUNS204195374
Company Name1929803 Ontario Corp
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusMR Unsafe
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchfalse
Serial Numbertrue
Manufacturing Datetrue
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone705-626-6419
Emailaeibl@flosonicsmedical.com
Phone705-626-6419
Emailaeibl@flosonicsmedical.com
Phone705-626-6419
Emailaeibl@flosonicsmedical.com
Phone705-626-6419
Emailaeibl@flosonicsmedical.com
Phone705-626-6419
Emailaeibl@flosonicsmedical.com
Phone705-626-6419
Emailaeibl@flosonicsmedical.com
Phone705-626-6419
Emailaeibl@flosonicsmedical.com
Phone705-626-6419
Emailaeibl@flosonicsmedical.com
Phone705-626-6419
Emailaeibl@flosonicsmedical.com
Phone705-626-6419
Emailaeibl@flosonicsmedical.com
Phone705-626-6419
Emailaeibl@flosonicsmedical.com
Phone705-626-6419
Emailaeibl@flosonicsmedical.com
Phone705-626-6419
Emailaeibl@flosonicsmedical.com
Phone705-626-6419
Emailaeibl@flosonicsmedical.com

Device Identifiers

Device Issuing AgencyDevice ID
GS110627987360100 [Primary]
GS120627987360114 [Package]
Contains: 10627987360100
Package: Box [10 Units]
In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

DPWFlowmeter, Blood, Cardiovascular

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2020-09-30
Device Publish Date2020-09-22

On-Brand Devices [FloPatch]

20627987360114FP120
00627987360103FP120

Trademark Results [FloPatch]

Mark Image

Registration | Serial
Company
Trademark
Application Date
FLOPATCH
FLOPATCH
88191780 not registered Live/Pending
1929803 Ontario Corp.
2018-11-13
FLOPATCH
FLOPATCH
87212425 not registered Dead/Abandoned
1929803 Ontario Corp.
2016-10-22

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