ATW Marker Wire Steerable Guidewires

Primary DI
20705032056561
Brand
ATW Marker Wire Steerable Guidewires
Company
CORDIS CORPORATION
Model
595EJ014
Catalog number
595EJ014
Device description
SGW ATW .014 J FLOPPY 195CM
Published
2021-01-26
Public version status
New
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true
OTC
false
Sterile
true
Single use
true

Product Codes#

Code, Name table
CodeName
DQXWire, guide, catheter

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
DQXWire, Guide, CatheterCardiovascular2

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K994358000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K994358000ATW MARKER WIRE STEERABLE GUIDEWIRECordis Corp.2000-01-13DQX

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
20705032056561PackageGS15In Commercial Distribution
10705032056564PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized table
Source identifierGTIN-14 normalized
2070503205656120705032056561
1070503205656410705032056564

GMDN Terms#

Term, Definition table
TermDefinition
Cardiac/peripheral vascular guidewire, single-useA long, thin, sterile wire intended to be percutaneously placed into the cardiac vasculature (ventricles or coronary vessels) to function as a guide for the introduction, positioning, and/or operation of a device (e.g., catheter, pacing lead); it may also be used in the peripheral vasculature. It may be made of metal (e.g., stainless steel, Nitinol), or polymer and/or glass materials to provide MRI-compatibility, with or without coating, and is available in a variety of distal tip designs. It is used for various diagnostic and interventional procedures, and may include devices used to facilitate manipulation (e.g., torque device). This is a single-use device.

Sterilization Methods#

Method table
Method

Regulatory Flags#

DUNS number
806136177
Device count
1
DM exempt
false
Premarket exempt
false
HCT/P
false
Kit
false
Combination product
false
Lot or batch
true
Serial number
false
Manufacturing date on label
false
Expiration date on label
true
Donation ID number
false
Contains natural rubber latex
false
No natural rubber latex
false
Sterilization required before use
false

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
10705032000109RAIN Sheath® Tibial Pedal IntroducerTP506510NTP506510N2023-05-05
10705032078900RAIN Sheath Transradial506516S506516S2018-10-09
10705032078917RAIN Sheath Transradial506510S506510S2018-10-09
10705032079020RAIN Sheath Transradial506516H506516H2018-10-09
10705032079044RAIN Sheath Transradial506410S506410S2018-10-09
10705032082051RAIN Sheath Transradial506716P20G506716P20G2020-12-17
10705032082099RAIN Sheath Transradial506716N506716N2020-12-17
10705032082181RAIN Sheath Transradial506410N506410N2020-12-17
10705032100007RAIN Sheath® Tibial Pedal IntroducerTP506510STP506510S2023-05-05
20705032081211Brite Tip Radianz6872801356872801352022-03-30
20705032081228Brite Tip Radianz6872801106872801102022-03-30
10705032076845RAILWAYRW5ADTBRW5ADTB2018-05-31
10705032076852RAILWAYRW5VBTHRW5VBTH2018-05-31
10705032076913RAILWAYRW7VBTHRW7VBTH2018-05-31
10705032076920RAILWAYRW7VBTBRW7VBTB2018-05-31
10705032019057VISTA BRITE TIP598941P598941P2024-02-23
10705032019170VISTA BRITE TIP598949P598949P2024-02-23
10705032020138VISTA BRITE TIP67004800670048002024-02-23
10705032042956VISTA BRITE TIPSM7497SM74972024-02-23
10705032043069VISTA BRITE TIPSM7540SM75402024-02-23

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