Locating Bar RT-4551BARMRI

GUDID 00841962119610

MR Safe Locating Bar

Qfix

Indexed-immobilization patient positioning system
Primary Device ID00841962119610
NIH Device Record Key6fdfd38d-74e1-49b7-9132-ac8d626c346d
Commercial Distribution StatusIn Commercial Distribution
Brand NameLocating Bar
Version Model NumberRT-4551BARMRI
Catalog NumberRT-4551BARMRI
Company DUNS808875397
Company NameQfix
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusMR Safe
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

Phone800-842-8688
Emailregulatory@cqmedical.com
Phone800-842-8688
Emailregulatory@cqmedical.com
Phone800-842-8688
Emailregulatory@cqmedical.com
Phone800-842-8688
Emailregulatory@cqmedical.com
Phone800-842-8688
Emailregulatory@cqmedical.com
Phone800-842-8688
Emailregulatory@cqmedical.com
Phone800-842-8688
Emailregulatory@cqmedical.com
Phone800-842-8688
Emailregulatory@cqmedical.com
Phone800-842-8688
Emailregulatory@cqmedical.com
Phone800-842-8688
Emailregulatory@cqmedical.com
Phone800-842-8688
Emailregulatory@cqmedical.com
Phone800-842-8688
Emailregulatory@cqmedical.com
Phone800-842-8688
Emailregulatory@cqmedical.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100841962119610 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

JAICouch, Radiation Therapy, Powered

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2025-07-17
Device Publish Date2025-07-09

On-Brand Devices [Locating Bar]

00841962119788Qfix Locating Bar
00841962119610MR Safe Locating Bar

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