FLYBROTHER

GUDID 06974830410534

Zhejiang Qianxi Vehicle Industry Co., Ltd.

Electric-motor-driven wheelchair, occupant-controlled
Primary Device ID06974830410534
NIH Device Record Key9e179946-ca91-4769-8856-e9aad9d02ae8
Commercial Distribution StatusIn Commercial Distribution
Brand NameFLYBROTHER
Version Model NumberXFGW30-107
Company DUNS527986033
Company NameZhejiang Qianxi Vehicle Industry Co., Ltd.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchtrue
Serial Numbertrue
Manufacturing Datetrue
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latextrue
RX Perscriptionfalse
OTC Over-The-Counterfalse

Customer Support Contacts

Phone3038000162
Emailwm06@chinaqianxi.com
Phone3038000162
Emailwm06@chinaqianxi.com
Phone3038000162
Emailwm06@chinaqianxi.com
Phone3038000162
Emailwm06@chinaqianxi.com
Phone3038000162
Emailwm06@chinaqianxi.com
Phone3038000162
Emailwm06@chinaqianxi.com
Phone3038000162
Emailwm06@chinaqianxi.com
Phone3038000162
Emailwm06@chinaqianxi.com
Phone3038000162
Emailwm06@chinaqianxi.com
Phone3038000162
Emailwm06@chinaqianxi.com
Phone3038000162
Emailwm06@chinaqianxi.com
Phone3038000162
Emailwm06@chinaqianxi.com
Phone3038000162
Emailwm06@chinaqianxi.com
Phone3038000162
Emailwm06@chinaqianxi.com
Phone3038000162
Emailwm06@chinaqianxi.com

Device Identifiers

Device Issuing AgencyDevice ID
GS106974830410534 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

ITIWheelchair, Powered

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2024-07-02
Device Publish Date2024-06-24

On-Brand Devices [FLYBROTHER]

06974830410572XFGW25-203
06974830410534XFGW30-107

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