Fibreplast® Variable Perf™ RT-1889KYFORF5

GUDID 10841962116128

Fibreplast 5-Point Mask, 3.2 mm, Variable Perf

Qfix

Patient positioning thermoplastic mould material
Primary Device ID10841962116128
NIH Device Record Key09c736d7-3b31-485e-a9e0-2dcb036bca52
Commercial Distribution StatusIn Commercial Distribution
Brand NameFibreplast® Variable Perf™
Version Model NumberRT-1889KYFORF5
Catalog NumberRT-1889KYFORF5
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
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
Depth3.2 Millimeter
Depth3.2 Millimeter
Depth3.2 Millimeter

Device Identifiers

Device Issuing AgencyDevice ID
GS110841962116128 [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 Date2021-12-27
Device Publish Date2021-12-17

On-Brand Devices [Fibreplast® Variable Perf™]

10841962117255Fibreplast VP HD+Shldr Portrait S-Frame, 3.2mm
10841962117231Fibreplast VP HD+Shldr Portrait S-Frame, 3.2mm
10841962117224Fibreplast Variable Perf, Head & Shoulder CURVE S-Frame, 3.2 mm
10841962117200Fibreplast Variable Perf, Head & Shoulder CURVE S-Frame, 3.2 mm
10841962116203Fibreplast VP Hd Only Portrait S-Frame, Std. 3.2mm
10841962116180Fibreplast VP Hd Only Portrait S-Frame, Std. 3.2mm
10841962116173Fibreplast VP, Slim U-Frame, Std. 3.2mm
10841962116159Fibreplast VP, Slim U-Frame, Std. 3.2mm
10841962116142Fibreplast 5-Point Mask, 3.2 mm, Variable Perf
10841962116128Fibreplast 5-Point Mask, 3.2 mm, Variable Perf
10841962116111Fibreplast 3-Point Mask, 3.2 mm, Variable Perf
10841962116098Fibreplast 3-Point Mask, 3.2 mm, Variable Perf
10841962116081Fibreplast Variable Perf, Head Only CURVE S-Frame, 3.2 mm, Standard
10841962116067Fibreplast Variable Perf, Head Only CURVE S-Frame, 3.2 mm, Standard
10841962110126Fibreplast 5-Point Mask, 3.2 mm, Variable Perf
10841962110119Fibreplast 3-Point Mask, 3.2 mm, Variable Perf

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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