iSnare 00711089

GUDID 10724995180826

The iSnare hexagonal system is a dual lumen device providing both needle injection and monopolar electrocautery polypectomy snare capability within a single catheter device.

US Endoscopy

Endoscopic electrosurgical submucosal lift/resection set
Primary Device ID10724995180826
NIH Device Record Keyc2564734-e9af-42b5-83d4-aa2bbef2ecb4
Commercial Distribution StatusIn Commercial Distribution
Brand NameiSnare
Version Model Number00711089
Catalog Number00711089
Company DUNS627879687
Company NameUS Endoscopy
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 Datetrue
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latextrue
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(800)548-4873
Emailxx@xx.xx
Phone+1(800)548-4873
Emailxx@xx.xx
Phone+1(800)548-4873
Emailxx@xx.xx
Phone+1(800)548-4873
Emailxx@xx.xx
Phone+1(800)548-4873
Emailxx@xx.xx

Device Dimensions

Width2.5 Millimeter
Length230 Centimeter
Needle Gauge23 Gauge
Width2.5 Millimeter
Length230 Centimeter
Needle Gauge23 Gauge
Width2.5 Millimeter
Length230 Centimeter
Needle Gauge23 Gauge
Width2.5 Millimeter
Length230 Centimeter
Needle Gauge23 Gauge
Width2.5 Millimeter

Operating and Storage Conditions

Storage Environment TemperatureBetween 15 Degrees Celsius and 25 Degrees Celsius
Special Storage Condition, SpecifyBetween 0 and 0 *Keep Dry
Special Storage Condition, SpecifyBetween 0 and 0 *Keep Dry
Special Storage Condition, SpecifyBetween 0 and 0 *Keep Dry
Special Storage Condition, SpecifyBetween 0 and 0 *Keep Dry

Device Identifiers

Device Issuing AgencyDevice ID
GS100724995180829 [Primary]
GS100816765010945 [Previous]
GS110724995180826 [Package]
Contains: 00724995180829
Package: Case [5 Units]
In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

FDISNARE, FLEXIBLE

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2020-03-27
Device Publish Date2020-03-19

On-Brand Devices [iSnare]

10816765012748The iSnare system–Lariat snare is used to inject various types of media and to grasp, dissect
10816765010942The iSnare hexagonal system is a dual lumen device providing both needle injection and monopolar
10816765010935The iSnare hexagonal system is a dual lumen device providing both needle injection and monopolar
10816765010928The iSnare oval system is a dual lumen device providing both needle injection and monopolar elec
10816765010911The iSnare system is a dual lumen device providing both needle injection and monopolar electroca
10724995180826The iSnare hexagonal system is a dual lumen device providing both needle injection and monopolar
10724995180819The iSnare hexagonal system is a dual lumen device providing both needle injection and monopolar
10724995180802The iSnare oval system is a dual lumen device providing both needle injection and monopolar elec
10724995180796The iSnare system is a dual lumen device providing both needle injection and monopolar electroca
10724995180789The iSnare system–Lariat snare is used to inject various types of media and to grasp, dissect

Trademark Results [iSnare]

Mark Image

Registration | Serial
Company
Trademark
Application Date
ISNARE
ISNARE
78646927 3331109 Live/Registered
U.S. Endoscopy Group, Inc.
2005-06-09

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