Halo™ Single Loop Snare Kit 383625120

GUDID 00886333224913

Halo™ Single Loop Snare Kit 6F, 25mm x 120cm

ARGON MEDICAL DEVICES, INC.

Intravascular catheter-snare Intravascular catheter-snare Intravascular catheter-snare Intravascular catheter-snare Intravascular catheter-snare Intravascular catheter-snare Intravascular catheter-snare Intravascular catheter-snare Intravascular catheter-snare Intravascular catheter-snare Intravascular catheter-snare Intravascular catheter-snare Intravascular catheter-snare Intravascular catheter-snare Intravascular catheter-snare Intravascular catheter-snare Intravascular extraction catheter-snare Intravascular extraction catheter-snare Intravascular extraction catheter-snare Intravascular extraction catheter-snare Intravascular extraction catheter-snare Intravascular extraction catheter-snare Intravascular extraction catheter-snare Intravascular extraction catheter-snare Intravascular extraction catheter-snare Intravascular extraction catheter-snare Intravascular extraction catheter-snare Intravascular extraction catheter-snare
Primary Device ID00886333224913
NIH Device Record Key2319314f-5faa-466e-939b-dba2f139dabb
Commercial Distribution StatusIn Commercial Distribution
Brand NameHalo™ Single Loop Snare Kit
Version Model Number383625120
Catalog Number383625120
Company DUNS140727624
Company NameARGON MEDICAL DEVICES, INC.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kittrue
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datetrue
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone1.800.927.4669
EmailCustomer.Service@argonmedical.com
Phone1.800.927.4669
EmailCustomer.Service@argonmedical.com
Phone1.800.927.4669
EmailCustomer.Service@argonmedical.com
Phone1.800.927.4669
EmailCustomer.Service@argonmedical.com
Phone1.800.927.4669
EmailCustomer.Service@argonmedical.com
Phone1.800.927.4669
EmailCustomer.Service@argonmedical.com
Phone1.800.927.4669
EmailCustomer.Service@argonmedical.com
Phone1.800.927.4669
EmailCustomer.Service@argonmedical.com
Phone1.800.927.4669
EmailCustomer.Service@argonmedical.com
Phone1.800.927.4669
EmailCustomer.Service@argonmedical.com
Phone1.800.927.4669
EmailCustomer.Service@argonmedical.com
Phone1.800.927.4669
EmailCustomer.Service@argonmedical.com
Phone1.800.927.4669
EmailCustomer.Service@argonmedical.com
Phone1.800.927.4669
EmailCustomer.Service@argonmedical.com
Phone1.800.927.4669
EmailCustomer.Service@argonmedical.com
Phone1.800.927.4669
EmailCustomer.Service@argonmedical.com
Phone1.800.927.4669
EmailCustomer.Service@argonmedical.com
Phone1.800.927.4669
EmailCustomer.Service@argonmedical.com
Phone1.800.927.4669
EmailCustomer.Service@argonmedical.com
Phone1.800.927.4669
EmailCustomer.Service@argonmedical.com
Phone1.800.927.4669
EmailCustomer.Service@argonmedical.com
Phone1.800.927.4669
EmailCustomer.Service@argonmedical.com
Phone1.800.927.4669
EmailCustomer.Service@argonmedical.com
Phone1.800.927.4669
EmailCustomer.Service@argonmedical.com
Phone1.800.927.4669
EmailCustomer.Service@argonmedical.com
Phone1.800.927.4669
EmailCustomer.Service@argonmedical.com
Phone1.800.927.4669
EmailCustomer.Service@argonmedical.com
Phone1.800.927.4669
EmailCustomer.Service@argonmedical.com

Device Dimensions

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Operating and Storage Conditions

Special Storage Condition, SpecifyBetween 0 and 0 *Keep dry and away from sunlight
Special Storage Condition, SpecifyBetween 0 and 0 *Keep dry and away from sunlight
Special Storage Condition, SpecifyBetween 0 and 0 *Keep dry and away from sunlight
Special Storage Condition, SpecifyBetween 0 and 0 *Keep dry and away from sunlight
Special Storage Condition, SpecifyBetween 0 and 0 *Keep dry and away from sunlight
Special Storage Condition, SpecifyBetween 0 and 0 *Keep dry and away from sunlight
Special Storage Condition, SpecifyBetween 0 and 0 *Keep dry and away from sunlight
Special Storage Condition, SpecifyBetween 0 and 0 *Keep dry and away from sunlight
Special Storage Condition, SpecifyBetween 0 and 0 *Keep dry and away from sunlight
Special Storage Condition, SpecifyBetween 0 and 0 *Keep dry and away from sunlight
Special Storage Condition, SpecifyBetween 0 and 0 *Keep dry and away from sunlight
Special Storage Condition, SpecifyBetween 0 and 0 *Keep dry and away from sunlight
Special Storage Condition, SpecifyBetween 0 and 0 *Keep dry and away from sunlight
Special Storage Condition, SpecifyBetween 0 and 0 *Keep dry and away from sunlight
Special Storage Condition, SpecifyBetween 0 and 0 *Keep dry and away from sunlight
Special Storage Condition, SpecifyBetween 0 and 0 *Keep dry and away from sunlight
Special Storage Condition, SpecifyBetween 0 and 0 *Keep dry and away from sunlight
Special Storage Condition, SpecifyBetween 0 and 0 *Keep dry and away from sunlight
Special Storage Condition, SpecifyBetween 0 and 0 *Keep dry and away from sunlight
Special Storage Condition, SpecifyBetween 0 and 0 *Keep dry and away from sunlight
Special Storage Condition, SpecifyBetween 0 and 0 *Keep dry and away from sunlight
Special Storage Condition, SpecifyBetween 0 and 0 *Keep dry and away from sunlight
Special Storage Condition, SpecifyBetween 0 and 0 *Keep dry and away from sunlight
Special Storage Condition, SpecifyBetween 0 and 0 *Keep dry and away from sunlight
Special Storage Condition, SpecifyBetween 0 and 0 *Keep dry and away from sunlight
Special Storage Condition, SpecifyBetween 0 and 0 *Keep dry and away from sunlight
Special Storage Condition, SpecifyBetween 0 and 0 *Keep dry and away from sunlight
Special Storage Condition, SpecifyBetween 0 and 0 *Keep dry and away from sunlight

Device Identifiers

Device Issuing AgencyDevice ID
GS100886333224913 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

MMXDevice, Percutaneous Retrieval

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2021-01-14
Device Publish Date2021-01-06

On-Brand Devices [Halo™ Single Loop Snare Kit]

00886333224937Halo™ Single Loop Snare Kit 6F, 35mm x 120cm
00886333224920Halo™ Single Loop Snare Kit 6F, 30mm x 120cm
00886333224913Halo™ Single Loop Snare Kit 6F, 25mm x 120cm
00886333224906Halo™ Single Loop Snare Kit 6F, 25mm x 65cm
00886333224890Halo™ Single Loop Snare Kit 6F, 20mm x 120cm
00886333224883Halo™ Single Loop Snare Kit 6F, 15mm x 120cm
00886333224876Halo™ Single Loop Snare Kit 4F, 10mm x 120cm
00886333224869Halo™ Single Loop Snare Kit 4F, 10mm x 65cm
00886333224852Halo™ Single Loop Snare Kit 4F, 5mm x 20cm

Trademark Results [Halo]

Mark Image

Registration | Serial
Company
Trademark
Application Date
HALO
HALO
98529116 not registered Live/Pending
WH Products, LLC
2024-05-01
HALO
HALO
98473348 not registered Live/Pending
Ultradent Products, Inc.
2024-03-28
HALO
HALO
98454522 not registered Live/Pending
Halo, Inc.
2024-03-18
HALO
HALO
98404978 not registered Live/Pending
Prophetic, Inc.
2024-02-14
HALO
HALO
98398702 not registered Live/Pending
Halo Water Systems, LLC
2024-02-08
HALO
HALO
98381032 not registered Live/Pending
CenTex Aerospace, Inc.
2024-01-29
HALO
HALO
98363520 not registered Live/Pending
Grace O'Donnell
2024-01-18
HALO
HALO
98342492 not registered Live/Pending
REJOICE INTERNATIONAL CORP.
2024-01-04
HALO
HALO
98317855 not registered Live/Pending
American Baitworks Co.
2023-12-16
HALO
HALO
98312564 not registered Live/Pending
Maars Holding B.V.
2023-12-13
HALO
HALO
98294381 not registered Live/Pending
NEXALIN TECHNOLOGY, INC.
2023-12-01
HALO
HALO
98230495 not registered Live/Pending
Halo Technologies, Inc
2023-10-19

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