EXPRO ELITE 8404

GUDID 30841156101590

Expro Elite Snare V2 35mm

TELEFLEX INCORPORATED

Intravascular extraction catheter-snare Intravascular extraction catheter-snare Intravascular extraction catheter-snare Intravascular extraction catheter-snare Intravascular extraction catheter-snare Intravascular extraction catheter-snare Intravascular extraction catheter-snare Intravascular extraction catheter-snare Intravascular extraction catheter-snare Intravascular extraction catheter-snare Intravascular extraction catheter-snare Intravascular extraction catheter-snare Intravascular extraction catheter-snare Intravascular extraction catheter-snare Intravascular extraction catheter-snare Intravascular extraction catheter-snare Intravascular extraction catheter-snare Intravascular extraction catheter-snare Intravascular extraction catheter-snare Intravascular extraction catheter-snare Intravascular extraction catheter-snare Intravascular extraction catheter-snare Intravascular extraction catheter-snare Intravascular extraction catheter-snare Intravascular extraction catheter-snare Intravascular extraction catheter-snare Intravascular extraction catheter-snare Intravascular extraction catheter-snare Intravascular extraction catheter-snare
Primary Device ID30841156101590
NIH Device Record Keybb28fa4a-5d13-48f3-9f91-ef2fe19d93a9
Commercial Distribution StatusIn Commercial Distribution
Brand NameEXPRO ELITE
Version Model NumberIPN913622
Catalog Number8404
Company DUNS002348191
Company NameTELEFLEX INCORPORATED
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kittrue
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(919)544-8000
EmailCS@TELEFLEX.COM
Phone+1(919)544-8000
EmailCS@TELEFLEX.COM
Phone+1(919)544-8000
EmailCS@TELEFLEX.COM
Phone+1(919)544-8000
EmailCS@TELEFLEX.COM
Phone+1(919)544-8000
EmailCS@TELEFLEX.COM
Phone+1(919)544-8000
EmailCS@TELEFLEX.COM
Phone+1(919)544-8000
EmailCS@TELEFLEX.COM
Phone+1(919)544-8000
EmailCS@TELEFLEX.COM
Phone+1(919)544-8000
EmailCS@TELEFLEX.COM
Phone+1(919)544-8000
EmailCS@TELEFLEX.COM
Phone+1(919)544-8000
EmailCS@TELEFLEX.COM
Phone+1(919)544-8000
EmailCS@TELEFLEX.COM
Phone+1(919)544-8000
EmailCS@TELEFLEX.COM
Phone+1(919)544-8000
EmailCS@TELEFLEX.COM
Phone+1(919)544-8000
EmailCS@TELEFLEX.COM
Phone+1(919)544-8000
EmailCS@TELEFLEX.COM
Phone+1(919)544-8000
EmailCS@TELEFLEX.COM
Phone+1(919)544-8000
EmailCS@TELEFLEX.COM
Phone+1(919)544-8000
EmailCS@TELEFLEX.COM
Phone+1(919)544-8000
EmailCS@TELEFLEX.COM
Phone+1(919)544-8000
EmailCS@TELEFLEX.COM
Phone+1(919)544-8000
EmailCS@TELEFLEX.COM
Phone+1(919)544-8000
EmailCS@TELEFLEX.COM
Phone+1(919)544-8000
EmailCS@TELEFLEX.COM
Phone+1(919)544-8000
EmailCS@TELEFLEX.COM
Phone+1(919)544-8000
EmailCS@TELEFLEX.COM
Phone+1(919)544-8000
EmailCS@TELEFLEX.COM
Phone+1(919)544-8000
EmailCS@TELEFLEX.COM
Phone+1(919)544-8000
EmailCS@TELEFLEX.COM

Device Dimensions

Width35 Millimeter
Width35 Millimeter
Width35 Millimeter
Width35 Millimeter
Width35 Millimeter
Width35 Millimeter
Width35 Millimeter
Width35 Millimeter
Width35 Millimeter
Width35 Millimeter
Width35 Millimeter
Width35 Millimeter
Width35 Millimeter
Width35 Millimeter
Width35 Millimeter
Width35 Millimeter
Width35 Millimeter
Width35 Millimeter
Width35 Millimeter
Width35 Millimeter
Width35 Millimeter
Width35 Millimeter
Width35 Millimeter
Width35 Millimeter
Width35 Millimeter
Width35 Millimeter
Width35 Millimeter
Width35 Millimeter
Width35 Millimeter

Device Identifiers

Device Issuing AgencyDevice ID
GS110841156101596 [Primary]
GS130841156101590 [Package]
Contains: 10841156101596
Package: Box [1 Units]
In Commercial Distribution

FDA Product Code

MMXDevice, percutaneous retrieval

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2021-07-08
Device Publish Date2018-11-08

On-Brand Devices [EXPRO ELITE]

30841156101583Expro Elite Snare V1 35mm
30841156101569Expro Elite Snare V1 25mm
30841156101545Expro Elite Snare V1 15mm
30841156101521Expro Elite Snare V1 10mm
30841156101507Expro Elite Snare V1 5mm
30841156101590Expro Elite Snare V2 35mm
30841156101576Expro Elite Snare V2 25mm
30841156101552Expro Elite Snare V2 15mm
30841156101538Expro Elite Snare V2 10mm
30841156101514Expro Elite Snare V2 5mm
© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.