ULTIMATEbros 3

GUDID 14547327084571

ASAHI INTECC CO., LTD.

Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use
Primary Device ID14547327084571
NIH Device Record Key18d99d4e-a509-46c2-887a-fd98c8a403ab
Commercial Distribution StatusIn Commercial Distribution
Brand NameULTIMATEbros 3
Version Model NumberAHW14S003J
Company DUNS690711189
Company NameASAHI INTECC CO., LTD.
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

Device Dimensions

Outer Diameter0.014 Inch
Outer Diameter0.014 Inch
Length180 Centimeter
Outer Diameter0.014 Inch
Length180 Centimeter
Outer Diameter0.014 Inch
Length180 Centimeter
Outer Diameter0.014 Inch
Length180 Centimeter
Outer Diameter0.014 Inch
Length180 Centimeter
Outer Diameter0.014 Inch
Length180 Centimeter
Outer Diameter0.014 Inch
Length180 Centimeter
Outer Diameter0.014 Inch
Length180 Centimeter
Outer Diameter0.014 Inch
Length180 Centimeter
Outer Diameter0.014 Inch
Length180 Centimeter
Outer Diameter0.014 Inch
Length180 Centimeter
Outer Diameter0.014 Inch
Length180 Centimeter
Outer Diameter0.014 Inch
Length180 Centimeter
Outer Diameter0.014 Inch
Length180 Centimeter
Outer Diameter0.014 Inch
Length180 Centimeter
Outer Diameter0.014 Inch
Length180 Centimeter
Outer Diameter0.014 Inch
Length180 Centimeter
Outer Diameter0.014 Inch
Length180 Centimeter
Outer Diameter0.014 Inch
Length180 Centimeter
Outer Diameter0.014 Inch
Length180 Centimeter
Outer Diameter0.014 Inch
Length180 Centimeter
Outer Diameter0.014 Inch
Length180 Centimeter
Outer Diameter0.014 Inch
Length180 Centimeter
Outer Diameter0.014 Inch
Length180 Centimeter
Outer Diameter0.014 Inch
Length180 Centimeter
Outer Diameter0.014 Inch
Length180 Centimeter
Outer Diameter0.014 Inch
Length180 Centimeter
Outer Diameter0.014 Inch
Length180 Centimeter
Outer Diameter0.014 Inch
Length180 Centimeter
Outer Diameter0.014 Inch
Length180 Centimeter
Outer Diameter0.014 Inch

Device Identifiers

Device Issuing AgencyDevice ID
GS104547327084574 [Primary]
GS114547327084571 [Package]
Contains: 04547327084574
Package: [5 Units]
In Commercial Distribution

FDA Product Code

DQXWIRE, GUIDE, CATHETER

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number5
Public Version Date2019-11-22
Device Publish Date2016-09-16

On-Brand Devices [ULTIMATEbros 3]

14547327084588AHW14S303J
14547327084571AHW14S003J
14547327084564AHW14S303S
14547327084557AHW14S003S
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