RunWay™

Primary DI
08714729119609
Brand
RunWay™
Company
BOSTON SCIENTIFIC CORPORATION
Model
H7493896977A0
Device description
Guide Catheter
Published
2016-09-24
Public version status
Update
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
DQYCATHETER, PERCUTANEOUS

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
DQYCatheter, PercutaneousCardiovascular2

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
08714729119609PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, EAN-13 table
Source identifierGTIN-14 normalizedEAN-13
08714729119609087147291196098714729119609

GMDN Terms#

Term, Definition table
TermDefinition
Vascular guide-catheter, single-useA flexible tube intended to be used for the percutaneous transluminal passage and placement of a diagnostic/interventional catheter, lead (e.g., pacing lead, balloon dilatation catheter), needle or guidewire through its lumen(s), within the vascular system. It may be rigid or flexible, non-steerable or steerable, single or multiple lumen(s), and the distal section can have a variety of preformed shapes. It is not intended solely for infusion nor to access superselective small vessels, and does not include a transseptal needle. A percutaneous introduction set, shaft visualization electrodes, or haemostatic valve may be supplied with the guide-catheter. This is a single-use device.

Device Sizes#

Type, Value, Unit table
TypeValueUnit
Device Size Text, specify0
Device Size Text, specify0

Regulatory Flags#

DUNS number
021717889
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
08714729832089Rubicon™ 18H749392390180902016-09-24
08714729832096Rubicon™ 35H749392400350902016-09-24
08714729832102Rubicon™ 35H749392400351502016-09-24
08714729832119Rubicon™ 35H749392400350602016-09-24
08714729832126Rubicon™ 35H749392400351302016-09-24
08714729832133Rubicon™ 14H749392120141302016-09-24
08714729832140Rubicon™ 14H749392120141502016-09-24
08714729832157Rubicon™ 18H749392390181302016-09-24
08714729832164Rubicon™ 18H749392390181502016-09-24
08714729118442Mach1™H7493435719D02016-09-24
08714729119203Mach1™H74934356103A02016-09-24
08714729119210Mach1™H7493435619C02016-09-24
08714729119227Mach1™H7493435677A02016-09-24
08714729119234Mach1™H7493435737P02016-09-24
08714729119241Mach1™H7493435737R02016-09-24
08714729119616RunWay™H7493896989A02016-09-24
08714729119715Mach1™H74934356108A02016-09-24
08714729119722Mach1™H74934356119A02016-09-24
08714729119739Mach1™H74934356104A02016-09-24
08714729119746Mach1™H74934356105A02016-09-24

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Primary DI, Brand, Company table
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00813132029562Quick-Cross Select Support CatheterPhilips Image Guided Therapy CorporationDQY2023-10-04
00813132029579Quick-Cross Select Support CatheterPhilips Image Guided Therapy CorporationDQY2023-10-04
00813132029586Quick-Cross Select Support CatheterPhilips Image Guided Therapy CorporationDQY2023-10-04
00813132029593Quick-Cross Select Support CatheterPhilips Image Guided Therapy CorporationDQY2023-10-04
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