Is this your brand? Sign in to claim ownership.

EV3, INC

Last updated May 24, 2026

Information

Country: US
Address: —
Website: medtronic.com
LinkedIn: —
Facebook: —
Email: [email protected]
Phone: +1(800)633-8766
PRRC Contact: —
EUDAMED SRN: —
FDA FEI Number: —
DUNS Number: 117446916

Catalogue (1096)

Page 5 of 22

Device	Model / Reference	Registries	Class	Status
EverCross™	AB35W06040080	FDA UDI	Class II	Active
Nitrex™	N181805	FDA UDI	Class II	Active
NanoCross™ Elite	AB14W050120090	FDA UDI	Class II	Active
EverCross™	AB35W06120040	FDA UDI	Class II	Active
EverFlex	PRB35-07-100-120	FDA UDI	Class III	Unknown
EverCross™	AB35W05030135	FDA UDI	Class II	Active
NanoCross™ Elite	AB14W035080150	FDA UDI	Class II	Active
Amplatz Goose Neck™	GN2501	FDA UDI	Class II	Active
NanoCross™ Elite	AB14W020060150	FDA UDI	Class II	Active
EverCross™	AB35W06150080	FDA UDI	Class II	Active
EverFlex™ Protégé™ EverFlex™	PRB35-07-150-120	FDA UDI	Class III	Active
Amplatz Goose Neck™	GN1001	FDA UDI	Class II	Active
EverCross™	AB35W03120135	FDA UDI	Class II	Active
Chocolate®	CB1413540120OTW	FDA UDI	Class II	Active
EverCross™	AB35W04060080	FDA UDI	Class II	Active
SpiderFX™	SPD2-US-070-190	FDA UDI	Class II	Unknown
NanoCross™ Elite	AB14W035120150	FDA UDI	Class II	Active
EverCross™	AB35W05080135	FDA UDI	Class II	Active
EverCross™	AB35W05030040	FDA UDI	Class II	Active
EverFlex	PRB35-06-020-080	FDA UDI	Class III	Unknown
NanoCross™ Elite	AB14W025100090	FDA UDI	Class II	Active
EverCross™	AB35W03080080	FDA UDI	Class II	Active
EverCross™	AB35W04150135	FDA UDI	Class II	Active
EverCross™	AB35W03040080	FDA UDI	Class II	Active
NanoCross™ Elite	AB14W060200150	FDA UDI	Class II	Active
EverCross™	AB35W04030080	FDA UDI	Class II	Active
NanoCross™ Elite	AB14W060100090	FDA UDI	Class II	Active
NanoCross™ Elite	AB14W035080150	FDA UDI	Class II	Active
EverCross™	AB35W12060135	FDA UDI	Class II	Active
NanoCross™ Elite	AB14W015040150	FDA UDI	Class II	Active
EverFlex™ Protégé™ EverFlex™	PRB35-06-150-120	FDA UDI	Class III	Active
NanoCross™ Elite	AB14W060120090	FDA UDI	Class II	Active
Nitrex™	N351454	FDA UDI	Class II	Active
EverCross™	AB35W06100080	FDA UDI	Class II	Active
NanoCross™ Elite	AB14W050100150	FDA UDI	Class II	Active
EverCross™	AB35W08020040	FDA UDI	Class II	Active
EverCross™	AB35W04060080	FDA UDI	Class II	Active
EverCross™	AB35W05020040	FDA UDI	Class II	Active
EverCross™	AB35W04080135	FDA UDI	Class II	Active
Amplatz Goose Neck™	SK201	FDA UDI	Class II	Active
NanoCross™ Elite	AB14W020210090	FDA UDI	Class II	Active
NanoCross™ Elite	AB14W035150090	FDA UDI	Class II	Active
NanoCross™ Elite	AB14W040020090	FDA UDI	Class II	Active
EverFlex	PRB35-06-120-080	FDA UDI	Class II	Active
EverFlex™ Protégé™ EverFlex™	PRB35-07-080-080	FDA UDI	Class III	Active
EverCross™	AB35W04030135	FDA UDI	Class II	Active
NanoCross™ Elite	AB14W050060090	FDA UDI	Class II	Active
EverCross™	AB35W03030080	FDA UDI	Class II	Active
NanoCross™ Elite	AB14W030150150	FDA UDI	Class II	Active
EverCross™	AB35W05200080	FDA UDI	Class II	Active

Related Companies

Authorised Representatives

No authorised representatives on record.

Importers

Not available yet.

Notified Bodies

Not available yet.

Authorities

Not available yet.

FDA Recalls (1)

Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.

Date	Recall No.	Class	Status	Reason
Mar 29, 2016	Z-1552-2016	—	terminated	Medtronic is conducting a voluntary Urgent Medical Device Recall of two lots of the PowerCross 0.018" Over the Wire (OTW) Percutaneous Transluminal Angioplasty (PTA) Dilatation Catheter because the product is mislabeled.