Amplatz Goose Neck™

FDA UDI

Class II (US FDA UDI)

by Medtronic, Inc.

Identity

Trade Name: Amplatz Goose Neck™ FDA UDI
Generic Name: Intravascular extraction catheter-snare FDA UDI
Device Name: SNARE GN1001 GOOSENECK SNARE V02 FDA UDI
Model / Reference: GN1001 FDA UDI
Description: SNARE GN1001 GOOSENECK SNARE V02 FDA UDI

Identifiers

Primary DI / UDI-DI: 00763000762377 FDA UDI
510(k) Number: K241259 FDA UDI
FDA Product Code: DXE FDA UDI
MMX FDA UDI
GMDN Term: Intravascular extraction catheter-snare FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 870.5150 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Dimensions & Sizes

Size: Catheter Gauge — 4.2 French FDA UDI
Catheter Inner Diameter — 1.02 Millimeter FDA UDI
Catheter Working Length — 48.0 Centimeter FDA UDI

Category: Intravascular extraction catheter-snare

Amplatz Goose Neck™ by Medtronic, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Intravascular extraction catheter-snare.

ONE Snare® — Merit Medical Systems, Inc. · Class II
NCircle — COOK INCORPORATED · Class I
EN Snare® — Merit Medical Systems, Inc. · Class II
ONO Retrieval Device — Onocor LLC · Class II
Halo™ Single-Loop Microsnare Kit — Argon Medical Devices, Inc. · Class II
Halo™ Single-Loop Microsnare Kit — Argon Medical Devices, Inc. · Class II
EMPOWER™ — Merit Medical Systems, Inc. · Class II
Atrieve™ Vascular Snare Kit — Argon Medical Devices, Inc. · Class II

Cleared under the same submission

K241259 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Medtronic, Inc.

Sources (1)

FDA UDI 1d898f64-cce6-48d4-a25b-838528ccb1e2 37 fields · synced May 30, 2026