Primary Device ID | 00841962119535 |
NIH Device Record Key | 4b334182-2553-4e6a-9b59-f02709086e38 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | AirShuttle Locating Bar |
Version Model Number | RT-5100-11 |
Catalog Number | RT-5100-11 |
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 | false |
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 | 800-842-8688 |
regulatory@cqmedical.com | |
Phone | 800-842-8688 |
regulatory@cqmedical.com | |
Phone | 800-842-8688 |
regulatory@cqmedical.com | |
Phone | 800-842-8688 |
regulatory@cqmedical.com | |
Phone | 800-842-8688 |
regulatory@cqmedical.com | |
Phone | 800-842-8688 |
regulatory@cqmedical.com | |
Phone | 800-842-8688 |
regulatory@cqmedical.com | |
Phone | 800-842-8688 |
regulatory@cqmedical.com | |
Phone | 800-842-8688 |
regulatory@cqmedical.com | |
Phone | 800-842-8688 |
regulatory@cqmedical.com | |
Phone | 800-842-8688 |
regulatory@cqmedical.com | |
Phone | 800-842-8688 |
regulatory@cqmedical.com | |
Phone | 800-842-8688 |
regulatory@cqmedical.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00841962119535 [Primary] |
FRZ | Device, Patient Transfer, Powered |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2025-07-17 |
Device Publish Date | 2025-07-09 |
00841962119535 | AirShuttle Locating Bar, Varian Compatible |
00841962119528 | AirShuttle Locating Bar, Elekta Compatible |