Aquaplast™ with Integrated Shim™ RT-A892SD

GUDID 10841962107072

Aquaplast Hd & Shldr Portrait S-Frame, 3.2mm , Std Perf w/ Integrated Shim

Qfix

Patient positioning thermoplastic mould material Patient positioning thermoplastic mould material Patient positioning thermoplastic mould material Patient positioning thermoplastic mould material Patient positioning thermoplastic mould material Patient positioning thermoplastic mould material Patient positioning thermoplastic mould material Patient positioning thermoplastic mould material Patient positioning thermoplastic mould material Patient positioning thermoplastic mould material Patient positioning thermoplastic mould material Patient positioning thermoplastic mould material Patient positioning thermoplastic mould material Patient positioning thermoplastic mould material Patient positioning thermoplastic mould material Patient positioning thermoplastic mould material Patient positioning thermoplastic mould material Patient positioning thermoplastic mould material Patient positioning thermoplastic mould material Patient positioning thermoplastic mould material Patient positioning thermoplastic mould material Patient positioning thermoplastic mould material Patient positioning thermoplastic mould material Patient positioning thermoplastic mould material Patient positioning thermoplastic mould material Patient positioning thermoplastic mould material Patient positioning thermoplastic mould material Patient positioning thermoplastic mould material Patient positioning thermoplastic mould material Patient positioning thermoplastic mould material Patient positioning thermoplastic mould material
Primary Device ID10841962107072
NIH Device Record Key5ea4b002-9ceb-4e2f-9852-322a62134844
Commercial Distribution StatusIn Commercial Distribution
Brand NameAquaplast™ with Integrated Shim™
Version Model NumberRT-A892SD
Catalog NumberRT-A892SD
Company DUNS808875397
Company NameQfix
Device Count5
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 Datefalse
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

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

Device Identifiers

Device Issuing AgencyDevice ID
GS110841962107072 [Primary]
GS110841962107089 [Unit of Use]

FDA Product Code

IYEAccelerator, linear, medical

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number5
Public Version Date2023-12-06
Device Publish Date2016-12-22

On-Brand Devices [Aquaplast™ with Integrated Shim™]

10841962117873Aquaplast RT Hd Only Portrait S-Frame, 2.4mm Std Perf w/ Integrated Shim
10841962117859Aquaplast RT Hd Only Portrait S-Frame, 2.4mm Std Perf w/ Integrated Shim
10841962107102Aquaplast RT Hd Only Portrait S-Frame, 2.4mm Std Perf w/ Integrated Shim
10841962107096Aquaplast RT Hd Only Portrait S-Frame, 2.4mm Std Perf w/ Integrated Shim
10841962110683Aquaplast RT Hd+Shldr Portrait S-Frame, 3.2mm Std Perf w/ Integrated Shim
10841962107072Aquaplast Hd & Shldr Portrait S-Frame, 3.2mm , Std Perf w/ Integrated Shim
10841962107065Aquaplast Hd & Shldr Portrait S-Frame, 3.2mm , Std Perf w/ Integrated Shim

Trademark Results [Aquaplast]

Mark Image

Registration | Serial
Company
Trademark
Application Date
AQUAPLAST
AQUAPLAST
97652650 not registered Live/Pending
Techniart Spolka Z.O.O.
2022-10-28
AQUAPLAST
AQUAPLAST
78918621 3239437 Dead/Cancelled
Standard Screen Supply Corp.
2006-06-28
AQUAPLAST
AQUAPLAST
76331748 2744140 Dead/Cancelled
Hi-Gear Products, Inc.
2001-10-29
AQUAPLAST
AQUAPLAST
74290876 1762658 Live/Registered
PERFORMANCE HEALTH HOLDINGS, INC.
1992-07-01

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