Single-Loop Snare Retrieval Kit 380911120

GUDID 00886333224609

Single-Loop Snare Retrieval Kit

ARGON MEDICAL DEVICES, INC.

Vena cava filter extraction/repositioning kit Vena cava filter extraction/repositioning kit Vena cava filter extraction/repositioning kit Vena cava filter extraction/repositioning kit Vena cava filter extraction/repositioning kit Vena cava filter extraction/repositioning kit Vena cava filter extraction/repositioning kit Vena cava filter extraction/repositioning kit Vena cava filter extraction/repositioning kit Vena cava filter extraction/repositioning kit Vena cava filter extraction/repositioning kit Vena cava filter extraction/repositioning kit Vena cava filter extraction/repositioning kit Vena cava filter extraction/repositioning kit Vena cava filter extraction/repositioning kit Vena cava filter extraction/repositioning kit
Primary Device ID00886333224609
NIH Device Record Key05e40b91-4f73-41e0-9a94-132025b7f1bc
Commercial Distribution StatusIn Commercial Distribution
Brand NameSingle-Loop Snare Retrieval Kit
Version Model Number380911120
Catalog Number380911120
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

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

Device Identifiers

Device Issuing AgencyDevice ID
GS100886333224609 [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 Date2021-06-24
Device Publish Date2021-06-16

Devices Manufactured by ARGON MEDICAL DEVICES, INC.

00886333227167 - CLEANER Vac™2024-04-25 CLEANER Vac™ Thrombectomy System - 18F OD x 115cm
00886333227174 - Cleaner Vac™2024-04-25 Cleaner Vac™ - 18F OD x 115cm Aspiration Catheter with Handpiece
00886333227624 - Cleaner Vac™2024-04-25 Cleaner Vac™ Aspiration Canister
00886333225743 - Kodiak2023-07-10 Kodiak™ Dual Port Coaxial Introducer Kit
20886333227284 - Co-Axial Introducer Needle2023-06-16 Co-Axial Introducer Needle 15ga x 6.8cm
20886333227383 - Percutaneous Introducer2023-04-19 Percutaneous Introducer with Depth Marks 4F x 25cm
20886333227390 - Percutaneous Introducer2023-04-19 Percutaneous Introducer with Depth Marks 4F x 45cm
20886333227406 - Percutaneous Introducer2023-04-19 Percutaneous Introducer with Depth Marks 4F x 65cm
© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.