CONFIANZA PRO 8-20 235cm Straight

GUDID 14547327138274

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 Cardiac/peripheral vascular guidewire, single-use
Primary Device ID14547327138274
NIH Device Record Key3f6405a5-bd24-4dbb-a215-a1280cd7228f
Commercial Distribution StatusIn Commercial Distribution
Brand NameCONFIANZA PRO 8-20 235cm Straight
Version Model NumberAGH143292
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

Length235 Centimeter
Outer Diameter0.014 Inch
Length235 Centimeter
Outer Diameter0.014 Inch
Length235 Centimeter
Outer Diameter0.014 Inch
Length235 Centimeter
Outer Diameter0.014 Inch
Length235 Centimeter
Outer Diameter0.014 Inch
Length235 Centimeter
Outer Diameter0.014 Inch
Length235 Centimeter
Outer Diameter0.014 Inch
Length235 Centimeter
Outer Diameter0.014 Inch
Length235 Centimeter
Outer Diameter0.014 Inch
Length235 Centimeter
Outer Diameter0.014 Inch
Length235 Centimeter
Outer Diameter0.014 Inch
Length235 Centimeter
Outer Diameter0.014 Inch
Length235 Centimeter
Outer Diameter0.014 Inch
Length235 Centimeter
Outer Diameter0.014 Inch
Length235 Centimeter
Outer Diameter0.014 Inch
Length235 Centimeter
Outer Diameter0.014 Inch

Device Identifiers

Device Issuing AgencyDevice ID
GS104547327138277 [Primary]
GS114547327138274 [Package]
Contains: 04547327138277
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 StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2022-01-24
Device Publish Date2022-01-16

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