Primary Device ID | 10841962117859 |
NIH Device Record Key | 4ccbe3ac-01c1-4d0a-b7df-49c56a5b1cb7 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Aquaplast™ with Integrated Shim™ |
Version Model Number | RT-A779SD |
Catalog Number | RT-A779SD |
Company DUNS | 808875397 |
Company Name | Qfix |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | MR Safe |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | true |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | +1(610)268-0585 |
Compliance@qfix.com | |
Phone | +1(610)268-0585 |
Compliance@qfix.com | |
Phone | +1(610)268-0585 |
Compliance@qfix.com | |
Phone | +1(610)268-0585 |
Compliance@qfix.com | |
Phone | +1(610)268-0585 |
Compliance@qfix.com | |
Phone | +1(610)268-0585 |
Compliance@qfix.com | |
Phone | +1(610)268-0585 |
Compliance@qfix.com | |
Phone | +1(610)268-0585 |
Compliance@qfix.com | |
Phone | +1(610)268-0585 |
Compliance@qfix.com | |
Phone | +1(610)268-0585 |
Compliance@qfix.com | |
Phone | +1(610)268-0585 |
Compliance@qfix.com | |
Phone | +1(610)268-0585 |
Compliance@qfix.com | |
Phone | +1(610)268-0585 |
Compliance@qfix.com | |
Phone | +1(610)268-0585 |
Compliance@qfix.com | |
Phone | +1(610)268-0585 |
Compliance@qfix.com | |
Phone | +1(610)268-0585 |
Compliance@qfix.com | |
Phone | +1(610)268-0585 |
Compliance@qfix.com | |
Phone | +1(610)268-0585 |
Compliance@qfix.com | |
Phone | +1(610)268-0585 |
Compliance@qfix.com | |
Phone | +1(610)268-0585 |
Compliance@qfix.com | |
Phone | +1(610)268-0585 |
Compliance@qfix.com | |
Phone | +1(610)268-0585 |
Compliance@qfix.com | |
Phone | +1(610)268-0585 |
Compliance@qfix.com | |
Phone | +1(610)268-0585 |
Compliance@qfix.com | |
Phone | +1(610)268-0585 |
Compliance@qfix.com | |
Phone | +1(610)268-0585 |
Compliance@qfix.com | |
Phone | +1(610)268-0585 |
Compliance@qfix.com | |
Phone | +1(610)268-0585 |
Compliance@qfix.com | |
Phone | +1(610)268-0585 |
Compliance@qfix.com | |
Phone | +1(610)268-0585 |
Compliance@qfix.com | |
Phone | +1(610)268-0585 |
Compliance@qfix.com | |
Phone | +1(610)268-0585 |
Compliance@qfix.com | |
Phone | +1(610)268-0585 |
Compliance@qfix.com | |
Phone | +1(610)268-0585 |
Compliance@qfix.com | |
Phone | +1(610)268-0585 |
Compliance@qfix.com | |
Phone | +1(610)268-0585 |
Compliance@qfix.com | |
Phone | +1(610)268-0585 |
Compliance@qfix.com | |
Phone | +1(610)268-0585 |
Compliance@qfix.com | |
Phone | +1(610)268-0585 |
Compliance@qfix.com | |
Phone | +1(610)268-0585 |
Compliance@qfix.com | |
Phone | +1(610)268-0585 |
Compliance@qfix.com | |
Phone | +1(610)268-0585 |
Compliance@qfix.com |
Depth | 2.4 Millimeter |
Depth | 2.4 Millimeter |
Depth | 2.4 Millimeter |
Depth | 2.4 Millimeter |
Depth | 2.4 Millimeter |
Depth | 2.4 Millimeter |
Depth | 2.4 Millimeter |
Depth | 2.4 Millimeter |
Depth | 2.4 Millimeter |
Depth | 2.4 Millimeter |
Depth | 2.4 Millimeter |
Depth | 2.4 Millimeter |
Depth | 2.4 Millimeter |
Depth | 2.4 Millimeter |
Depth | 2.4 Millimeter |
Depth | 2.4 Millimeter |
Depth | 2.4 Millimeter |
Depth | 2.4 Millimeter |
Depth | 2.4 Millimeter |
Depth | 2.4 Millimeter |
Depth | 2.4 Millimeter |
Depth | 2.4 Millimeter |
Depth | 2.4 Millimeter |
Depth | 2.4 Millimeter |
Depth | 2.4 Millimeter |
Depth | 2.4 Millimeter |
Depth | 2.4 Millimeter |
Depth | 2.4 Millimeter |
Depth | 2.4 Millimeter |
Depth | 2.4 Millimeter |
Depth | 2.4 Millimeter |
Depth | 2.4 Millimeter |
Depth | 2.4 Millimeter |
Depth | 2.4 Millimeter |
Depth | 2.4 Millimeter |
Depth | 2.4 Millimeter |
Depth | 2.4 Millimeter |
Depth | 2.4 Millimeter |
Depth | 2.4 Millimeter |
Depth | 2.4 Millimeter |
Depth | 2.4 Millimeter |
Depth | 2.4 Millimeter |
Device Issuing Agency | Device ID |
---|---|
GS1 | 10841962117859 [Primary] |
IYE | Accelerator, linear, medical |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2021-12-28 |
Device Publish Date | 2021-12-20 |
10841962117873 | Aquaplast RT Hd Only Portrait S-Frame, 2.4mm Std Perf w/ Integrated Shim |
10841962117859 | Aquaplast RT Hd Only Portrait S-Frame, 2.4mm Std Perf w/ Integrated Shim |
10841962107102 | Aquaplast RT Hd Only Portrait S-Frame, 2.4mm Std Perf w/ Integrated Shim |
10841962107096 | Aquaplast RT Hd Only Portrait S-Frame, 2.4mm Std Perf w/ Integrated Shim |
10841962110683 | Aquaplast RT Hd+Shldr Portrait S-Frame, 3.2mm Std Perf w/ Integrated Shim |
10841962107072 | Aquaplast Hd & Shldr Portrait S-Frame, 3.2mm , Std Perf w/ Integrated Shim |
10841962107065 | Aquaplast Hd & Shldr Portrait S-Frame, 3.2mm , Std Perf w/ Integrated Shim |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
AQUAPLAST 97652650 not registered Live/Pending |
Techniart Spolka Z.O.O. 2022-10-28 |
AQUAPLAST 78918621 3239437 Dead/Cancelled |
Standard Screen Supply Corp. 2006-06-28 |
AQUAPLAST 76331748 2744140 Dead/Cancelled |
Hi-Gear Products, Inc. 2001-10-29 |
AQUAPLAST 74290876 1762658 Live/Registered |
PERFORMANCE HEALTH HOLDINGS, INC. 1992-07-01 |