ConvertX™ Nephroureteral Stent System 100010-20

GUDID 00851571007208

BRIGHTWATER MEDICAL, INC.

Polymeric ureteral stent Polymeric ureteral stent Polymeric ureteral stent Polymeric ureteral stent Polymeric ureteral stent Polymeric ureteral stent Polymeric ureteral stent Polymeric ureteral stent Polymeric ureteral stent Polymeric ureteral stent Polymeric ureteral stent Polymeric ureteral stent Polymeric ureteral stent Polymeric ureteral stent Polymeric ureteral stent Polymeric ureteral stent Polymeric ureteral stent Polymeric ureteral stent Polymeric ureteral stent Polymeric ureteral stent Polymeric ureteral stent Polymeric ureteral stent Polymeric ureteral stent Polymeric ureteral stent Polymeric ureteral stent Polymeric ureteral stent Polymeric ureteral stent Polymeric ureteral stent Polymeric ureteral stent Polymeric ureteral stent Polymeric ureteral stent
Primary Device ID00851571007208
NIH Device Record Key0f1f5c8d-c07a-4fbb-9d20-9ebac944e401
Commercial Distribution StatusIn Commercial Distribution
Brand NameConvertX™ Nephroureteral Stent System
Version Model Number10.3F x 20cm
Catalog Number100010-20
Company DUNS080049659
Company NameBRIGHTWATER MEDICAL, INC.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusMR Conditional
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datetrue
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone9512903410
Emailxx@xx.xx
Phone9512903410
Emailxx@xx.xx
Phone9512903410
Emailxx@xx.xx
Phone9512903410
Emailxx@xx.xx
Phone9512903410
Emailxx@xx.xx
Phone9512903410
Emailxx@xx.xx
Phone9512903410
Emailxx@xx.xx
Phone9512903410
Emailxx@xx.xx
Phone9512903410
Emailxx@xx.xx
Phone9512903410
Emailxx@xx.xx
Phone9512903410
Emailxx@xx.xx
Phone9512903410
Emailxx@xx.xx
Phone9512903410
Emailxx@xx.xx
Phone9512903410
Emailxx@xx.xx
Phone9512903410
Emailxx@xx.xx
Phone9512903410
Emailxx@xx.xx
Phone9512903410
Emailxx@xx.xx
Phone9512903410
Emailxx@xx.xx
Phone9512903410
Emailxx@xx.xx
Phone9512903410
Emailxx@xx.xx
Phone9512903410
Emailxx@xx.xx
Phone9512903410
Emailxx@xx.xx
Phone9512903410
Emailxx@xx.xx
Phone9512903410
Emailxx@xx.xx
Phone9512903410
Emailxx@xx.xx
Phone9512903410
Emailxx@xx.xx
Phone9512903410
Emailxx@xx.xx
Phone9512903410
Emailxx@xx.xx
Phone9512903410
Emailxx@xx.xx
Phone9512903410
Emailxx@xx.xx
Phone9512903410
Emailxx@xx.xx

Device Dimensions

Length20 Centimeter
Length20 Centimeter
Catheter Gauge10.3 French
Length20 Centimeter
Catheter Gauge10.3 French
Length20 Centimeter
Catheter Gauge10.3 French
Length20 Centimeter
Catheter Gauge10.3 French
Length20 Centimeter
Catheter Gauge10.3 French
Length20 Centimeter
Catheter Gauge10.3 French
Length20 Centimeter
Catheter Gauge10.3 French
Length20 Centimeter
Catheter Gauge10.3 French
Length20 Centimeter
Catheter Gauge10.3 French
Length20 Centimeter
Catheter Gauge10.3 French
Length20 Centimeter
Catheter Gauge10.3 French
Length20 Centimeter
Catheter Gauge10.3 French
Length20 Centimeter
Catheter Gauge10.3 French
Length20 Centimeter
Catheter Gauge10.3 French
Length20 Centimeter
Catheter Gauge10.3 French
Length20 Centimeter
Catheter Gauge10.3 French
Length20 Centimeter
Catheter Gauge10.3 French
Length20 Centimeter
Catheter Gauge10.3 French
Length20 Centimeter
Catheter Gauge10.3 French
Length20 Centimeter
Catheter Gauge10.3 French
Length20 Centimeter
Catheter Gauge10.3 French
Length20 Centimeter
Catheter Gauge10.3 French
Length20 Centimeter
Catheter Gauge10.3 French
Length20 Centimeter
Catheter Gauge10.3 French
Length20 Centimeter
Catheter Gauge10.3 French
Length20 Centimeter
Catheter Gauge10.3 French
Length20 Centimeter
Catheter Gauge10.3 French
Length20 Centimeter
Catheter Gauge10.3 French
Length20 Centimeter
Catheter Gauge10.3 French
Length20 Centimeter
Catheter Gauge10.3 French
Length20 Centimeter

Device Identifiers

Device Issuing AgencyDevice ID
GS100851571007208 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

FADStent, Ureteral

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number4
Public Version Date2018-10-10
Device Publish Date2017-07-07

On-Brand Devices [ConvertX™ Nephroureteral Stent System]

008515710073838.3F - 10.3F Taper x 28cm
008515710073768.3F - 10.3F Taper x 26cm
008515710073698.3F - 10.3F Taper x 24cm
008515710073528.3F - 10.3F Taper x 22cm
008515710073458.3F - 10.3F Taper x 20cm
0085157100728410.3F x 28cm
0085157100726010.3F x 26cm
0085157100724610.3F x 24cm
0085157100722210.3F x 22cm
0085157100720810.3F x 20cm
008515710075368.3F - 10.3F Taper x 14cm
008515710075298.3F - 10.3F Taper x 12cm
008515710075128.3F - 10.3F Taper x 10cm
0085157100750510.3F x 14cm
0085157100749910.3F x 12cm
0085157100748210.3F x 10cm

Trademark Results [ConvertX]

Mark Image

Registration | Serial
Company
Trademark
Application Date
CONVERTX
CONVERTX
86534783 5601549 Live/Registered
BrightWater Medical, Inc.
2015-02-13
CONVERTX
CONVERTX
78267482 2926982 Dead/Cancelled
Shinano Kenshi Kabushiki Kaisha
2003-06-26

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