FDA.reportPublic FDA data

The Magnet™

Primary DI
08714729008828
Brand
The Magnet™
Company
BOSTON SCIENTIFIC CORPORATION
Model
H74908966050
Device description
Exchange Device
Published
2016-09-24
Public version status
Update
Distribution status
Not 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

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
08714729008828PackageGS15Not in Commercial Distribution
08714729724940PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, EAN-13 table
Source identifierGTIN-14 normalizedEAN-13
08714729008828087147290088288714729008828
08714729724940087147297249408714729724940

GMDN Terms#

Term, Definition table
TermDefinition
Catheter-exchange guidewire holderA sterile hand-held device intended for use during guidewire-assisted intravascular interventional procedures [e.g., percutaneous transluminal coronary angioplasty (PTCA)] to facilitate the exchange of one catheter for another (e.g., coronary angioplasty balloon catheter) while maintaining the position of the guidewire. It consists of a clip for mechanical attachment to part of the catheterization device set, and a magnetic channel through which the catheter/guidewire is passed to enable removal of the catheter while the metal guidewire is magnetically held in place. This is a single-use device.

Sterilization Methods#

Method table
Method

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
08714729749172RX Cholangiogram KitM005714802016-09-24
00191506020729iNod™ Ultrasound Guided Biopsy NeM00502060M005020602023-03-21
00191506020910iNod™ Ultrasound Guidance ConsoM00503210M005032102023-03-21
00191506020927iNod™ Ultrasound Guidance ConsoM0050321R0M0050321R02023-03-21
00191506020934iNod™M00503300M005033002023-03-21
00191506020941iNod™M0050330R0M0050330R02023-03-21
00191506021924iNod™M00503200M005032002023-03-21
00191506021931iNod™M0050320R0M0050320R02023-03-21
08714729860853Expel™ Drainage Catheter with Twist-Loc™ HubH74939341082502016-08-17
08714729860860Expel™ Drainage Catheter with Twist-Loc™ HubH74939341102502016-08-17
08714729860877Expel™ Drainage Catheter with Twist-Loc™ HubH74939341122502016-08-17
08714729860884Expel™ Drainage Catheter with Twist-Loc™ HubH74939341142502016-08-17
08714729860891Expel™ Drainage Catheter with Twist-Loc™ HubH749393410825K12016-08-17
08714729860907Expel™ Drainage Catheter with Twist-Loc™ HubH749393411025K12016-08-17
08714729860914Expel™ Drainage Catheter with Twist-Loc™ HubH749393411225K12016-08-17
00802526623400NA694669462024-08-29
00802526604430INGEVITY™+78402020-02-06
00802526604522INGEVITY™+78422020-02-06
00802526604577INGEVITY™+78412020-02-06
00802526480546NA662866282014-09-24

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