Pinnacle Radiation Therapy Planning System 45980171803X

GUDID 00884838103566

Philips Medical Systems (cleveland), Inc.

Radiation therapy software Radiation therapy software Radiation therapy software Radiation therapy software Radiation therapy software Radiation therapy software Radiation therapy software Radiation therapy software Radiation therapy software Radiation therapy software Radiation therapy software Radiation therapy software Radiation therapy software Radiation therapy software Radiation therapy software Radiation therapy software Radiation therapy software Radiation therapy software Radiation therapy software Radiation therapy software Radiation therapy software Radiation therapy software Radiation therapy software Radiation therapy software
Primary Device ID00884838103566
NIH Device Record Key2e67a5ab-77c8-42df-b029-3c974343bf73
Commercial Distribution Discontinuation2030-11-09
Commercial Distribution StatusIn Commercial Distribution
Brand NamePinnacle Radiation Therapy Planning System
Version Model Number18.0
Catalog Number45980171803X
Company DUNS829526560
Company NamePhilips Medical Systems (cleveland), Inc.
Device Count1
DM Exempttrue
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchtrue
Serial Numberfalse
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+1(800)722-9377
Emailpros.support@philips.com
Phone+1(800)722-9377
Emailpros.support@philips.com
Phone+1(800)722-9377
Emailpros.support@philips.com
Phone+1(800)722-9377
Emailpros.support@philips.com
Phone+1(800)722-9377
Emailpros.support@philips.com
Phone+1(800)722-9377
Emailpros.support@philips.com
Phone+1(800)722-9377
Emailpros.support@philips.com
Phone+1(800)722-9377
Emailpros.support@philips.com
Phone+1(800)722-9377
Emailpros.support@philips.com
Phone+1(800)722-9377
Emailpros.support@philips.com
Phone+1(800)722-9377
Emailpros.support@philips.com
Phone+1(800)722-9377
Emailpros.support@philips.com
Phone+1(800)722-9377
Emailpros.support@philips.com
Phone+1(800)722-9377
Emailpros.support@philips.com
Phone+1(800)722-9377
Emailpros.support@philips.com
Phone+1(800)722-9377
Emailpros.support@philips.com
Phone+1(800)722-9377
Emailpros.support@philips.com
Phone+1(800)722-9377
Emailpros.support@philips.com
Phone+1(800)722-9377
Emailpros.support@philips.com
Phone+1(800)722-9377
Emailpros.support@philips.com
Phone+1(800)722-9377
Emailpros.support@philips.com
Phone+1(800)722-9377
Emailpros.support@philips.com
Phone+1(800)722-9377
Emailpros.support@philips.com
Phone+1(800)722-9377
Emailpros.support@philips.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100884838103566 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

MUJSystem, planning, radiation therapy treatment

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2021-08-06
Device Publish Date2020-11-09

On-Brand Devices [Pinnacle Radiation Therapy Planning System ]

0088483810356618.0
0088483810296516.4

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