Fibreplast® Variable Perf™ Assure™ Open View with Integrated Shim™ RT-A892KYSDF

GUDID 10841962118030

Fibreplast Open View Hd+Shldr S-Frame 3.2mm Variable Perf w/ Integrated Shim

Qfix

Patient positioning thermoplastic mould material
Primary Device ID10841962118030
NIH Device Record Key27a963cf-be84-4f20-89e4-158e401709f9
Commercial Distribution StatusIn Commercial Distribution
Brand NameFibreplast® Variable Perf™ Assure™ Open View with Integrated Shim™
Version Model NumberRT-A892KYSDF
Catalog NumberRT-A892KYSDF
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 Usetrue
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(610)268-0585
EmailCompliance@qfix.com
Phone+1(610)268-0585
EmailCompliance@qfix.com
Phone+1(610)268-0585
EmailCompliance@qfix.com
Phone+1(610)268-0585
EmailCompliance@qfix.com
Phone+1(610)268-0585
EmailCompliance@qfix.com
Phone+1(610)268-0585
EmailCompliance@qfix.com
Phone+1(610)268-0585
EmailCompliance@qfix.com
Phone+1(610)268-0585
EmailCompliance@qfix.com
Phone+1(610)268-0585
EmailCompliance@qfix.com
Phone+1(610)268-0585
EmailCompliance@qfix.com
Phone+1(610)268-0585
EmailCompliance@qfix.com
Phone+1(610)268-0585
EmailCompliance@qfix.com
Phone+1(610)268-0585
EmailCompliance@qfix.com
Phone+1(610)268-0585
EmailCompliance@qfix.com
Phone+1(610)268-0585
EmailCompliance@qfix.com
Phone+1(610)268-0585
EmailCompliance@qfix.com
Phone+1(610)268-0585
EmailCompliance@qfix.com
Phone+1(610)268-0585
EmailCompliance@qfix.com
Phone+1(610)268-0585
EmailCompliance@qfix.com
Phone+1(610)268-0585
EmailCompliance@qfix.com
Phone+1(610)268-0585
EmailCompliance@qfix.com
Phone+1(610)268-0585
EmailCompliance@qfix.com
Phone+1(610)268-0585
EmailCompliance@qfix.com
Phone+1(610)268-0585
EmailCompliance@qfix.com
Phone+1(610)268-0585
EmailCompliance@qfix.com
Phone+1(610)268-0585
EmailCompliance@qfix.com
Phone+1(610)268-0585
EmailCompliance@qfix.com
Phone+1(610)268-0585
EmailCompliance@qfix.com
Phone+1(610)268-0585
EmailCompliance@qfix.com
Phone+1(610)268-0585
EmailCompliance@qfix.com
Phone+1(610)268-0585
EmailCompliance@qfix.com
Phone+1(610)268-0585
EmailCompliance@qfix.com
Phone+1(610)268-0585
EmailCompliance@qfix.com
Phone+1(610)268-0585
EmailCompliance@qfix.com
Phone+1(610)268-0585
EmailCompliance@qfix.com
Phone+1(610)268-0585
EmailCompliance@qfix.com
Phone+1(610)268-0585
EmailCompliance@qfix.com
Phone+1(610)268-0585
EmailCompliance@qfix.com
Phone+1(610)268-0585
EmailCompliance@qfix.com
Phone+1(610)268-0585
EmailCompliance@qfix.com
Phone+1(610)268-0585
EmailCompliance@qfix.com
Phone+1(610)268-0585
EmailCompliance@qfix.com
Phone+1(610)268-0585
EmailCompliance@qfix.com
Phone+1(610)268-0585
EmailCompliance@qfix.com

Device Dimensions

Depth3.2 Millimeter
Depth3.2 Millimeter
Depth3.2 Millimeter
Depth3.2 Millimeter
Depth3.2 Millimeter
Depth3.2 Millimeter
Depth3.2 Millimeter
Depth3.2 Millimeter
Depth3.2 Millimeter
Depth3.2 Millimeter
Depth3.2 Millimeter
Depth3.2 Millimeter
Depth3.2 Millimeter
Depth3.2 Millimeter
Depth3.2 Millimeter
Depth3.2 Millimeter
Depth3.2 Millimeter
Depth3.2 Millimeter
Depth3.2 Millimeter
Depth3.2 Millimeter
Depth3.2 Millimeter
Depth3.2 Millimeter
Depth3.2 Millimeter
Depth3.2 Millimeter
Depth3.2 Millimeter
Depth3.2 Millimeter
Depth3.2 Millimeter
Depth3.2 Millimeter
Depth3.2 Millimeter
Depth3.2 Millimeter
Depth3.2 Millimeter
Depth3.2 Millimeter
Depth3.2 Millimeter
Depth3.2 Millimeter
Depth3.2 Millimeter
Depth3.2 Millimeter
Depth3.2 Millimeter
Depth3.2 Millimeter
Depth3.2 Millimeter
Depth3.2 Millimeter
Depth3.2 Millimeter
Depth3.2 Millimeter
Depth3.2 Millimeter
Depth3.2 Millimeter

Device Identifiers

Device Issuing AgencyDevice ID
GS110841962118030 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

IYEAccelerator, linear, medical

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2021-12-28
Device Publish Date2021-12-20

On-Brand Devices [Fibreplast® Variable Perf™ Assure™ Open View with Integrated Shim™]

10841962118054Fibreplast Open View Hd+Shldr S-Frame 3.2mm Variable Perf w/ Integrated Shim
10841962118030Fibreplast Open View Hd+Shldr S-Frame 3.2mm Variable Perf w/ Integrated Shim

Trademark Results [Fibreplast]

Mark Image

Registration | Serial
Company
Trademark
Application Date
FIBREPLAST
FIBREPLAST
85862461 4414349 Live/Registered
Qfix Systems LLC
2013-02-28

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