Triever24 22-101/AS-0224

GUDID 00810123710096

INARI MEDICAL INC

Thrombectomy suction catheter
Primary Device ID00810123710096
NIH Device Record Key5bd05a13-8e24-4d09-9056-ce839073277a
Commercial Distribution StatusIn Commercial Distribution
Brand NameTriever24
Version Model Number22-101
Catalog Number22-101/AS-0224
Company DUNS076827459
Company NameINARI MEDICAL INC
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone18779234747
Emailinfo@inarimedical.com
Phone18779234747
Emailinfo@inarimedical.com
Phone18779234747
Emailinfo@inarimedical.com
Phone18779234747
Emailinfo@inarimedical.com
Phone18779234747
Emailinfo@inarimedical.com
Phone18779234747
Emailinfo@inarimedical.com
Phone18779234747
Emailinfo@inarimedical.com
Phone18779234747
Emailinfo@inarimedical.com
Phone18779234747
Emailinfo@inarimedical.com
Phone18779234747
Emailinfo@inarimedical.com
Phone18779234747
Emailinfo@inarimedical.com
Phone18779234747
Emailinfo@inarimedical.com
Phone18779234747
Emailinfo@inarimedical.com
Phone18779234747
Emailinfo@inarimedical.com
Phone18779234747
Emailinfo@inarimedical.com
Phone18779234747
Emailinfo@inarimedical.com
Phone18779234747
Emailinfo@inarimedical.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100810123710096 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

QEWPeripheral Mechanical Thrombectomy With Aspiration

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2024-04-25
Device Publish Date2024-04-17

Devices Manufactured by INARI MEDICAL INC

00810123710577 - Artix Thin-Walled Sheath2024-11-19 Artix Thin-Walled Sheath
00810123710584 - Artix MT2024-11-19 Artix MT (Thrombectomy Device)
00810123710591 - Artix MT2024-11-19 Artix MT (Thrombectomy Device)
00810123710560 - Artix Thin-Walled Sheath2024-11-15 Artix Thin-Walled Sheath (Thrombectomy Sheath)
00810123710478 - 16 Fr Evacuation System2024-10-18 16 Fr Evacuation System
00810123710485 - 24 Fr Evacuation System2024-10-18 24 Fr Evacuation System
00810123710546 - FlowSaver2024-06-06 FlowSaver
00810123710096 - Triever242024-04-25
00810123710096 - Triever242024-04-25

Trademark Results [Triever24]

Mark Image

Registration | Serial
Company
Trademark
Application Date
TRIEVER24
TRIEVER24
88269913 5939893 Live/Registered
Inari Medical Inc.
2019-01-21

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.