AlligatorTM

FDA UDI

Class II (US FDA UDI)

by Micro Therapeutics, Inc.

Identity

Trade Name: AlligatorTM FDA UDI
Generic Name: Intravascular extraction catheter-snare FDA UDI
Device Name: FA-88810-30 ALLIGATOR DEVICE ARD 3MM FDA UDI
Model / Reference: FA-88810-30 FDA UDI
Description: FA-88810-30 ALLIGATOR DEVICE ARD 3MM FDA UDI

Identifiers

Primary DI / UDI-DI: 00847536013018 FDA UDI
FDA Product Code: DQY FDA UDI
GMDN Term: Intravascular extraction catheter-snare FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 870.1250 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

Sterilization Method

Ethylene Oxide FDA UDI

Category: Intravascular extraction catheter-snare

AlligatorTM by Micro Therapeutics, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Halo™ Single-Loop Microsnare Kit — Argon Medical Devices, Inc. · Class II
Halo™ Single-Loop Microsnare Kit — Argon Medical Devices, Inc. · Class II

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: Micro Therapeutics, Inc.

Sources (1)

FDA UDI 38131415-033c-407b-aa85-bdf5afd7996c 35 fields · synced May 31, 2026