UROLIFT UL2-C

GUDID 20814932020340

UroLift 2 Implant Cartridge

TELEFLEX INCORPORATED

Prostatic retraction implant Prostatic retraction implant Prostatic retraction implant Prostatic retraction implant Prostatic retraction implant Prostatic retraction implant Prostatic retraction implant Prostatic retraction implant Prostatic retraction implant Prostatic retraction implant Prostatic retraction implant Prostatic retraction implant Prostatic retraction implant Prostatic retraction implant Prostatic retraction implant Prostatic retraction implant Prostatic retraction implant
Primary Device ID20814932020340
NIH Device Record Key5894acfe-41c9-4e8c-881d-ea662d341486
Commercial Distribution StatusIn Commercial Distribution
Brand NameUROLIFT
Version Model NumberIPN924184
Catalog NumberUL2-C
Company DUNS002348191
Company NameTELEFLEX INCORPORATED
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 Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(925)401-0700
EmailCS@TELEFLEX.COM
Phone+1(925)401-0700
EmailCS@TELEFLEX.COM
Phone+1(925)401-0700
EmailCS@TELEFLEX.COM
Phone+1(925)401-0700
EmailCS@TELEFLEX.COM
Phone+1(925)401-0700
EmailCS@TELEFLEX.COM
Phone+1(925)401-0700
EmailCS@TELEFLEX.COM
Phone+1(925)401-0700
EmailCS@TELEFLEX.COM
Phone+1(925)401-0700
EmailCS@TELEFLEX.COM
Phone+1(925)401-0700
EmailCS@TELEFLEX.COM
Phone+1(925)401-0700
EmailCS@TELEFLEX.COM
Phone+1(925)401-0700
EmailCS@TELEFLEX.COM
Phone+1(925)401-0700
EmailCS@TELEFLEX.COM
Phone+1(925)401-0700
EmailCS@TELEFLEX.COM
Phone+1(925)401-0700
EmailCS@TELEFLEX.COM
Phone+1(925)401-0700
EmailCS@TELEFLEX.COM
Phone+1(925)401-0700
EmailCS@TELEFLEX.COM
Phone+1(925)401-0700
EmailCS@TELEFLEX.COM

Device Identifiers

Device Issuing AgencyDevice ID
GS110814932020343 [Primary]
GS120814932020340 [Package]
Contains: 10814932020343
Package: Carton [4 Units]
In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

PEWImplantable transprostatic tissue retractor system

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2023-03-23
Device Publish Date2023-03-15

On-Brand Devices [UROLIFT]

10814932020084UroLift System
20814932020142UroLift ATC System
20814932020159UroLift System
20814932020135UroLift 2 Delivery Handle, U.S.
20814932020128UroLift 2 Implant Cartridge
00814932020056UROLIFT PROCEDURE KIT STERILIZATION TRAY
20814932020210UroLift System
10814932020206IPN056885
20814932020296UroLift 2 Implant Cartridge
20814932020289UroLift 2 Implant Cartridge Handle Kit
20814932020197UroLift System Rigid Retrieval Kit Sterilization Tray
20814932020272UroLift System
20814932020265UroLift System
20814932020357UroLift 2 Implant Cartridge Handle Kit
20814932020340UroLift 2 Implant Cartridge
20814932020395UroLift System
20814932020388UroLift System
20814932020401UroLift ATC System
20814932020364UroLift UL2 ATC Implant Cartridge
20814932020456UroLift UL2 ATC Implant Cartridge

Trademark Results [UROLIFT]

Mark Image

Registration | Serial
Company
Trademark
Application Date
UROLIFT
UROLIFT
87296231 5256109 Live/Registered
Neotract, Inc.
2017-01-10
UROLIFT
UROLIFT
77184568 3609328 Live/Registered
Neotract, Inc.
2007-05-18

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