FDA.reportPublic FDA data

Trapper™ Exchange Device

Primary DI
05391526210154
Brand
Trapper™ Exchange Device
Company
CREGANNA UNLIMITED COMPANY
Model
H74939330130
Catalog number
H74939330130
Device description
Trapper™ Exchange Device
Published
2017-01-27
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
DQYCatheter, Percutaneous

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
DQYCatheter, PercutaneousCardiovascular2

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
05391526210154PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, EAN-13 table
Source identifierGTIN-14 normalizedEAN-13
05391526210154053915262101545391526210154

GMDN Terms#

Term, Definition table
TermDefinition
Coronary angioplasty balloon catheter, basicA flexible tube designed for percutaneous transluminal coronary angioplasty (PTCA) to dilate a stenotic coronary artery by controlled inflation of a distensible balloon(s) at its distal tip. It is typically available as: 1) an over-the-wire (OTW) type that has a double or triple-lumen, one for the guidewire and one or two for single- or double-balloon inflation; and 2) a rapid exchange (RX) type with a single-lumen. It is available in various sizes for the dilatation of small, narrowed, or obstructed coronary arteries or bypass grafts. It may also be intended for pre- or post-dilatation of a balloon-expandable stent (not included) in the coronary arteries. This is a single-use device.

Device Sizes#

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

Sterilization Methods#

Method table
Method

Regulatory Flags#

DUNS number
985218606
Device count
1
Lot or batch
true
Expiration date on label
true

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
05391526210017Gore TIPS® SheathTSTH1040TSTH10402016-09-23
05391526210109Lotus™ Introducer SetH749NTR180LIS-S2016-09-23
05391526210116Lotus™ Introducer SetH749NTR200LIS-L2016-09-23
25391526210028Gore TIPS SetTSET1016TSET10162016-09-23
05391526210000Gore TIPS NeedleTNDL1656TNDL16562016-09-23
05391526210031Zurpaz™ Steerable Sheath SetM004EPTMC85300M004EPTMC853002016-09-23
05391526210048Zurpaz™ Steerable Sheath SetM004EPTMCA85400M004EPTMCA854002016-09-23
05391526210055Zurpaz™ Steerable Sheath SetM004USMC85100M004USMC851002016-09-23
05391526210062Zurpaz™ Steerable Sheath SetM004USMCA85200M004USMCA852002016-09-23
05391526210079Zurpaz™ Steerable Sheath SetM004JPNMC85500M004JPNMC855002016-09-23
05391526210086Zurpaz™ Steerable Sheath SetM004JPNMCA85600M004JPNMCA856002016-09-23
05391526210253Attain Assist™ CS Access Catheter 146168-01146168-012019-01-14

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Primary DI, Brand, Company table
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07613327623376AXS LiftStryker CorporationDQY2025-03-04
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