Fibreplast™ Micro Perf™ Assure™ Open View RT-1778KSDF
GUDID 10841962105337
Fibreplast Open View Hd +Shldr 2.4mm Micro Perf
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| Primary Device ID | 10841962105337 |
| NIH Device Record Key | f7b8b9ba-0ab9-4a34-aaa3-313a271d21d8 |
| 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 | 10 |
| 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 |
Device Dimensions
| 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 Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 10841962105337 [Primary] |
| GS1 | 10841962105344 [Unit of Use] |
FDA Pre-market Approvals/Notifications & deNovo
- Premarket Notification: K935067
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 | 4 |
| Public Version Date | 2020-02-18 |
| Device Publish Date | 2016-12-22 |
On-Brand Devices [Fibreplast™ Micro Perf™ Assure™ Open View]
| 10841962105337 | Fibreplast Open View Hd +Shldr 2.4mm Micro Perf |
| 10841962105320 | Fibreplast Open View Hd +Shldr 2.4mm Micro Perf |
Trademark Results [Fibreplast]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 FIBREPLAST 85862461 4414349 Live/Registered |
Qfix Systems LLC 2013-02-28 |
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