Primary Device ID | 10841962111956 |
NIH Device Record Key | 385c4014-86ca-4772-83a1-3dca0cca930a |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Fibreplast® Micro Perf™ Assure™ Open View |
Version Model Number | RT-1778KSDF |
Catalog Number | RT-1778KSDF |
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 | 10841962111956 [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 | 2021-12-22 |
Device Publish Date | 2021-12-14 |
10841962111970 | Fibreplast Open View Hd +Shldr 2.4mm Micro Perf |
10841962111956 | Fibreplast Open View Hd +Shldr 2.4mm Micro Perf |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
FIBREPLAST 85862461 4414349 Live/Registered |
Qfix Systems LLC 2013-02-28 |