CHIKAI black 18 soft tip

GUDID 24547327116910

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 ID24547327116910
NIH Device Record Key6a3c1f41-9322-4c4a-8779-0406e7e0be79
Commercial Distribution StatusIn Commercial Distribution
Brand NameCHIKAI black 18 soft tip
Version Model NumberAIN-CKI-18-200-SFT
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 Diameter0.018 Inch
Outer Diameter0.018 Inch
Length200 Centimeter
Outer Diameter0.018 Inch
Length200 Centimeter
Outer Diameter0.018 Inch
Length200 Centimeter
Outer Diameter0.018 Inch
Length200 Centimeter
Outer Diameter0.018 Inch
Length200 Centimeter
Outer Diameter0.018 Inch
Length200 Centimeter
Outer Diameter0.018 Inch
Length200 Centimeter
Outer Diameter0.018 Inch
Length200 Centimeter
Outer Diameter0.018 Inch
Length200 Centimeter
Outer Diameter0.018 Inch
Length200 Centimeter
Outer Diameter0.018 Inch
Length200 Centimeter
Outer Diameter0.018 Inch
Length200 Centimeter
Outer Diameter0.018 Inch
Length200 Centimeter
Outer Diameter0.018 Inch
Length200 Centimeter
Outer Diameter0.018 Inch
Length200 Centimeter
Outer Diameter0.018 Inch
Length200 Centimeter
Outer Diameter0.018 Inch
Length200 Centimeter
Outer Diameter0.018 Inch
Length200 Centimeter
Outer Diameter0.018 Inch
Length200 Centimeter
Outer Diameter0.018 Inch
Length200 Centimeter
Outer Diameter0.018 Inch
Length200 Centimeter
Outer Diameter0.018 Inch
Length200 Centimeter
Outer Diameter0.018 Inch
Length200 Centimeter
Outer Diameter0.018 Inch
Length200 Centimeter
Outer Diameter0.018 Inch
Length200 Centimeter
Outer Diameter0.018 Inch
Length200 Centimeter
Outer Diameter0.018 Inch
Length200 Centimeter
Outer Diameter0.018 Inch
Length200 Centimeter
Outer Diameter0.018 Inch
Length200 Centimeter
Outer Diameter0.018 Inch
Length200 Centimeter
Outer Diameter0.018 Inch

Device Identifiers

Device Issuing AgencyDevice ID
GS104547327116916 [Primary]
GS124547327116910 [Package]
Contains: 04547327116916
Package: [1 Units]
In Commercial Distribution

FDA Product Code

MOFGUIDE, WIRE, CATHETER, NEUROVASCULATURE

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 Date2017-08-21

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