MM-TSM 797418

GUDID 00845225012922

Multi-Modality Touch Screen Module

Philips Image Guided Therapy Corporation

Cardiovascular ultrasound imaging system Cardiovascular ultrasound imaging system Cardiovascular ultrasound imaging system Cardiovascular ultrasound imaging system Cardiovascular ultrasound imaging system Cardiovascular ultrasound imaging system Cardiovascular ultrasound imaging system Cardiovascular ultrasound imaging system Cardiovascular ultrasound imaging system Cardiovascular ultrasound imaging system Cardiovascular ultrasound imaging system Cardiovascular ultrasound imaging system Cardiovascular ultrasound imaging system Cardiovascular ultrasound imaging system Cardiovascular ultrasound imaging system Cardiovascular ultrasound imaging system
Primary Device ID00845225012922
NIH Device Record Key4426fc9c-a5ea-4c21-a7d5-4afb3ac378a9
Commercial Distribution StatusIn Commercial Distribution
Brand NameMM-TSM
Version Model Number797418
Catalog Number797418
Company DUNS018860556
Company NamePhilips Image Guided Therapy Corporation
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 Usefalse
Lot Batchfalse
Serial Numbertrue
Manufacturing Datetrue
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone(800) 228-4728
EmailIGTD.CustomerInquiry@philips.com
Phone(800) 228-4728
EmailIGTD.CustomerInquiry@philips.com
Phone(800) 228-4728
EmailIGTD.CustomerInquiry@philips.com
Phone(800) 228-4728
EmailIGTD.CustomerInquiry@philips.com
Phone(800) 228-4728
EmailIGTD.CustomerInquiry@philips.com
Phone(800) 228-4728
EmailIGTD.CustomerInquiry@philips.com
Phone(800) 228-4728
EmailIGTD.CustomerInquiry@philips.com
Phone(800) 228-4728
EmailIGTD.CustomerInquiry@philips.com
Phone(800) 228-4728
EmailIGTD.CustomerInquiry@philips.com
Phone(800) 228-4728
EmailIGTD.CustomerInquiry@philips.com
Phone(800) 228-4728
EmailIGTD.CustomerInquiry@philips.com
Phone(800) 228-4728
EmailIGTD.CustomerInquiry@philips.com
Phone(800) 228-4728
EmailIGTD.CustomerInquiry@philips.com
Phone(800) 228-4728
EmailIGTD.CustomerInquiry@philips.com
Phone(800) 228-4728
EmailIGTD.CustomerInquiry@philips.com
Phone(800) 228-4728
EmailIGTD.CustomerInquiry@philips.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100845225012922 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

DSACable, Transducer And Electrode, Patient, (Including Connector)

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2022-02-28
Device Publish Date2022-02-18

Devices Manufactured by Philips Image Guided Therapy Corporation

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20813132029429 - Quick-Cross Extreme2023-10-12 Quick-Cross Extreme Support Catheter
20813132029436 - Quick-Cross Extreme2023-10-12 Quick-Cross Extreme Support Catheter
20813132029443 - Quick-Cross Extreme2023-10-12 Quick-Cross Extreme Support Catheter
20813132029450 - Quick-Cross Extreme2023-10-12 Quick-Cross Extreme Support Catheter
00813132029463 - Quick-Cross Extreme2023-10-12 Quick-Cross Extreme Support Catheter
20813132029474 - Quick-Cross Extreme2023-10-12 Quick-Cross Extreme Support Catheter
20813132029481 - Quick-Cross Extreme2023-10-12 Quick-Cross Extreme Support Catheter
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