Dual Adhesive Strap

GUDID 10627987360148

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 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 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 ID10627987360148
NIH Device Record Key40227799-163e-48c3-b285-e91ae777cc43
Commercial Distribution StatusIn Commercial Distribution
Brand NameDual Adhesive Strap
Version Model NumberFP120-FOT01-005
Company DUNS204195374
Company Name1929803 Ontario Corp
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 Usetrue
Lot Batchtrue
Serial Numberfalse
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

Phone2899982982
Emailcchin@flosonicsmedical.com
Phone2899982982
Emailcchin@flosonicsmedical.com
Phone2899982982
Emailcchin@flosonicsmedical.com
Phone2899982982
Emailcchin@flosonicsmedical.com
Phone2899982982
Emailcchin@flosonicsmedical.com
Phone2899982982
Emailcchin@flosonicsmedical.com
Phone2899982982
Emailcchin@flosonicsmedical.com
Phone2899982982
Emailcchin@flosonicsmedical.com
Phone2899982982
Emailcchin@flosonicsmedical.com
Phone2899982982
Emailcchin@flosonicsmedical.com
Phone2899982982
Emailcchin@flosonicsmedical.com
Phone2899982982
Emailcchin@flosonicsmedical.com
Phone2899982982
Emailcchin@flosonicsmedical.com
Phone2899982982
Emailcchin@flosonicsmedical.com
Phone2899982982
Emailcchin@flosonicsmedical.com
Phone2899982982
Emailcchin@flosonicsmedical.com
Phone2899982982
Emailcchin@flosonicsmedical.com
Phone2899982982
Emailcchin@flosonicsmedical.com
Phone2899982982
Emailcchin@flosonicsmedical.com
Phone2899982982
Emailcchin@flosonicsmedical.com
Phone2899982982
Emailcchin@flosonicsmedical.com
Phone2899982982
Emailcchin@flosonicsmedical.com
Phone2899982982
Emailcchin@flosonicsmedical.com
Phone2899982982
Emailcchin@flosonicsmedical.com
Phone2899982982
Emailcchin@flosonicsmedical.com
Phone2899982982
Emailcchin@flosonicsmedical.com
Phone2899982982
Emailcchin@flosonicsmedical.com
Phone2899982982
Emailcchin@flosonicsmedical.com
Phone2899982982
Emailcchin@flosonicsmedical.com
Phone2899982982
Emailcchin@flosonicsmedical.com
Phone2899982982
Emailcchin@flosonicsmedical.com
Phone2899982982
Emailcchin@flosonicsmedical.com
Phone2899982982
Emailcchin@flosonicsmedical.com
Phone2899982982
Emailcchin@flosonicsmedical.com
Phone2899982982
Emailcchin@flosonicsmedical.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100627987360141 [Primary]
GS110627987360148 [Package]
Contains: 00627987360141
Package: Bag [10 Units]
In Commercial Distribution

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 Date2023-03-13
Device Publish Date2023-03-03

Devices Manufactured by 1929803 Ontario Corp

10627987360131 - Reprocess FloPatch2023-05-16
10627987360148 - Dual Adhesive Strap2023-03-13
10627987360148 - Dual Adhesive Strap2023-03-13
10627987360117 - Hydrogel Adhesive Strap2022-06-27
00627987360127 - Acrylate Adhesive Strap2022-06-27
00627987360103 - FloPatch2020-10-29
20627987360114 - FloPatch2020-09-30

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