FDA.reportPublic FDA data

INFINITI

Primary DI
10705032014939
Brand
INFINITI
Company
Cordis US Corp.
Model
538491P
Catalog number
538491P
Device description
CATH PRIMOPAC INF FR4 W/CSI
Published
2016-08-01
Public version status
Update
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true
Sterile
true
Single use
true

Product Codes#

Code, Name table
CodeName
DQOCATHETER, INTRAVASCULAR, DIAGNOSTIC
OEZCardiovascular Procedure Kit

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
DQOCatheter, Intravascular, DiagnosticCardiovascular2
OEZCardiovascular Procedure KitCardiovascular2

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K960975000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K9609750001-4F INFINITI ANGIOGRAPHIC CATHETERCordis Corp.1996-04-02DQO

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
20705032014936PackageGS110In Commercial Distribution
10705032014939PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized table
Source identifierGTIN-14 normalized
2070503201493620705032014936
1070503201493910705032014939

GMDN Terms#

Term, Definition table
TermDefinition
Angiographic catheter, single-useA thin, flexible tube designed to inject a contrast medium into select blood vessels of the cerebral, visceral, or peripheral vasculature during an angiographic procedure in order to facilitate the clear visualization of the vascular system of a targeted organ or area of the body. It is introduced percutaneously, has a radiopaque marker(s) for positioning, and may include disposable devices dedicated to catheter introduction/function [e.g., sheath(s)]. It may also be used for simultaneous pressure measurements to determine the transvalvular, intravascular, and intraventricular pressure gradients. This is a single-use device.

Storage And Handling#

Type, Low, High table
TypeLowHighCondition
Storage Environment Temperature15 Degrees Celsius30 Degrees Celsius

Sterilization Methods#

Method table
Method

Regulatory Flags#

DUNS number
118274128
Device count
1
Premarket exempt
true
Lot or batch
true
Expiration date on label
true
No natural rubber latex
true

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
10705032100557VISTA BRITE TIP588-842PM588-842PM2024-09-09
10705032100571VISTA BRITE TIP670-052-00M670-052-00M2024-09-09
10705032100595VISTA BRITE TIP670-002-00M670-002-00M2024-09-09
10705032100618VISTA BRITE TIP778-054-00M778-054-00M2024-09-09
10705032100625VISTA BRITE TIP670-034-00M670-034-00M2024-09-09
10705032100649VISTA BRITE TIP670-083-00M670-083-00M2024-09-09
10705032100656VISTA BRITE TIP778-052-00M778-052-00M2024-09-09
10705032100663VISTA BRITE TIP778-082-00M778-082-00M2024-09-09
10705032100670VISTA BRITE TIP670-036-00M670-036-00M2024-09-09
10705032100694VISTA BRITE TIP556-082-0LM556-082-0LM2024-09-09
10705032100700VISTA BRITE TIP670-110-00M670-110-00M2024-09-09
10705032100731VISTA BRITE TIP670-112-00M670-112-00M2024-09-09
10705032100748VISTA BRITE TIP670-190-00M670-190-00M2024-09-09
10705032100755VISTA BRITE TIP778-055-00M778-055-00M2024-09-09
10705032100762VISTA BRITE TIP670-055-00M670-055-00M2024-09-09
10705032100779VISTA BRITE TIP556-002-0LM556-002-0LM2024-09-09
10705032100793VISTA BRITE TIP556-080-0LM556-080-0LM2024-09-09
10705032100809VISTA BRITE TIP670-005-00M670-005-00M2024-09-09
10705032100816VISTA BRITE TIP556-054-0LM556-054-0LM2024-09-09
10705032100823VISTA BRITE TIP778-037-00M778-037-00M2024-09-09

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Primary DI, Brand, Company table
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