6.0FR (2mm) X 20 cm DOUBLE PIGTAIL URETERAL STENT TECOFLEX™

GUDID 00821925005457

serving as a temporary indwelling catheter.

Gyrus Acmi, Inc.

Polymeric ureteral stent
Primary Device ID00821925005457
NIH Device Record Keyce98b742-a9ec-4e6e-ad2d-c449aa78aede
Commercial Distribution StatusIn Commercial Distribution
Brand Name6.0FR (2mm) X 20 cm DOUBLE PIGTAIL URETERAL STENT TECOFLEX™
Version Model Number5616020
Company DUNS007198742
Company NameGyrus Acmi, Inc.
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 Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone18885247266
Emailxxx@xxx.xxx
Phone18885247266
Emailxxx@xxx.xxx
Phone18885247266
Emailxxx@xxx.xxx
Phone18885247266
Emailxxx@xxx.xxx
Phone18885247266
Emailxxx@xxx.xxx
Phone18885247266
Emailxxx@xxx.xxx
Phone18885247266
Emailxxx@xxx.xxx
Phone18885247266
Emailxxx@xxx.xxx
Phone18885247266
Emailxxx@xxx.xxx
Phone18885247266
Emailxxx@xxx.xxx
Phone18885247266
Emailxxx@xxx.xxx
Phone18885247266
Emailxxx@xxx.xxx
Phone18885247266
Emailxxx@xxx.xxx
Phone18885247266
Emailxxx@xxx.xxx
Phone18885247266
Emailxxx@xxx.xxx
Phone18885247266
Emailxxx@xxx.xxx
Phone18885247266
Emailxxx@xxx.xxx
Phone18885247266
Emailxxx@xxx.xxx
Phone18885247266
Emailxxx@xxx.xxx

Device Identifiers

Device Issuing AgencyDevice ID
GS100821925005457 [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 Number3
Public Version Date2018-07-06
Device Publish Date2015-10-24

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