Aquaplast™ with Integrated Shim™ RT-A892SD
GUDID 10841962110683
Aquaplast RT Hd+Shldr Portrait S-Frame, 3.2mm Std Perf w/ Integrated Shim
Qfix
Patient positioning thermoplastic mould material| Primary Device ID | 10841962110683 |
| NIH Device Record Key | 7a6fafbe-21a1-4101-b5b3-cde80e1a1780 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Aquaplast™ with Integrated Shim™ |
| Version Model Number | RT-A892SD |
| Catalog Number | RT-A892SD |
| Company DUNS | 808875397 |
| Company Name | Qfix |
| Device Count | 5 |
| 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 | false |
| 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 |
Customer Support Contacts
| 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 |
Device Dimensions
| Depth | 3.2 Millimeter |
| Depth | 3.2 Millimeter |
| Depth | 3.2 Millimeter |
| Depth | 3.2 Millimeter |
| Depth | 3.2 Millimeter |
| Depth | 3.2 Millimeter |
| Depth | 3.2 Millimeter |
| Depth | 3.2 Millimeter |
| Depth | 3.2 Millimeter |
| Depth | 3.2 Millimeter |
| Depth | 3.2 Millimeter |
| Depth | 3.2 Millimeter |
| Depth | 3.2 Millimeter |
| Depth | 3.2 Millimeter |
| Depth | 3.2 Millimeter |
| Depth | 3.2 Millimeter |
| Depth | 3.2 Millimeter |
| Depth | 3.2 Millimeter |
| Depth | 3.2 Millimeter |
| Depth | 3.2 Millimeter |
| Depth | 3.2 Millimeter |
| Depth | 3.2 Millimeter |
| Depth | 3.2 Millimeter |
| Depth | 3.2 Millimeter |
| Depth | 3.2 Millimeter |
| Depth | 3.2 Millimeter |
| Depth | 3.2 Millimeter |
| Depth | 3.2 Millimeter |
| Depth | 3.2 Millimeter |
| Depth | 3.2 Millimeter |
| Depth | 3.2 Millimeter |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 10841962110683 [Primary] |
| GS1 | 10841962110690 [Unit of Use] |
FDA Product Code
| IYE | Accelerator, linear, medical |
Sterilization
| Steralize Prior To Use | false |
| Device Is Sterile | false |
Device Entry Metadata
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2023-12-06 |
| Device Publish Date | 2018-02-28 |
On-Brand Devices [Aquaplast™ with Integrated Shim™]
| 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 |
Trademark Results [Aquaplast]
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 |
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