Primary Device ID | 00850291007215 |
NIH Device Record Key | 92b8666e-27b3-44b9-95b4-2bdb44c37cc2 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Triever 20 Curve |
Version Model Number | 21-201 |
Company DUNS | 076827459 |
Company Name | INARI MEDICAL INC |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | 949-600-8433 |
info@inarimedical.com | |
Phone | 949-600-8433 |
info@inarimedical.com | |
Phone | 949-600-8433 |
info@inarimedical.com | |
Phone | 949-600-8433 |
info@inarimedical.com | |
Phone | 949-600-8433 |
info@inarimedical.com | |
Phone | 949-600-8433 |
info@inarimedical.com | |
Phone | 949-600-8433 |
info@inarimedical.com | |
Phone | 949-600-8433 |
info@inarimedical.com | |
Phone | 949-600-8433 |
info@inarimedical.com | |
Phone | 949-600-8433 |
info@inarimedical.com | |
Phone | 949-600-8433 |
info@inarimedical.com | |
Phone | 949-600-8433 |
info@inarimedical.com | |
Phone | 949-600-8433 |
info@inarimedical.com | |
Phone | 949-600-8433 |
info@inarimedical.com | |
Phone | 949-600-8433 |
info@inarimedical.com | |
Phone | 949-600-8433 |
info@inarimedical.com | |
Phone | 949-600-8433 |
info@inarimedical.com | |
Phone | 949-600-8433 |
info@inarimedical.com | |
Phone | 949-600-8433 |
info@inarimedical.com | |
Phone | 949-600-8433 |
info@inarimedical.com | |
Phone | 949-600-8433 |
info@inarimedical.com | |
Phone | 949-600-8433 |
info@inarimedical.com | |
Phone | 949-600-8433 |
info@inarimedical.com |
Outer Diameter | 6.5 Millimeter |
Catheter Working Length | 105 Centimeter |
Outer Diameter | 6.5 Millimeter |
Catheter Working Length | 105 Centimeter |
Outer Diameter | 6.5 Millimeter |
Catheter Working Length | 105 Centimeter |
Outer Diameter | 6.5 Millimeter |
Catheter Working Length | 105 Centimeter |
Outer Diameter | 6.5 Millimeter |
Catheter Working Length | 105 Centimeter |
Outer Diameter | 6.5 Millimeter |
Catheter Working Length | 105 Centimeter |
Outer Diameter | 6.5 Millimeter |
Catheter Working Length | 105 Centimeter |
Outer Diameter | 6.5 Millimeter |
Catheter Working Length | 105 Centimeter |
Outer Diameter | 6.5 Millimeter |
Catheter Working Length | 105 Centimeter |
Outer Diameter | 6.5 Millimeter |
Catheter Working Length | 105 Centimeter |
Outer Diameter | 6.5 Millimeter |
Catheter Working Length | 105 Centimeter |
Outer Diameter | 6.5 Millimeter |
Catheter Working Length | 105 Centimeter |
Outer Diameter | 6.5 Millimeter |
Catheter Working Length | 105 Centimeter |
Outer Diameter | 6.5 Millimeter |
Catheter Working Length | 105 Centimeter |
Outer Diameter | 6.5 Millimeter |
Catheter Working Length | 105 Centimeter |
Outer Diameter | 6.5 Millimeter |
Catheter Working Length | 105 Centimeter |
Outer Diameter | 6.5 Millimeter |
Catheter Working Length | 105 Centimeter |
Outer Diameter | 6.5 Millimeter |
Catheter Working Length | 105 Centimeter |
Outer Diameter | 6.5 Millimeter |
Catheter Working Length | 105 Centimeter |
Outer Diameter | 6.5 Millimeter |
Catheter Working Length | 105 Centimeter |
Outer Diameter | 6.5 Millimeter |
Catheter Working Length | 105 Centimeter |
Outer Diameter | 6.5 Millimeter |
Catheter Working Length | 105 Centimeter |
Outer Diameter | 6.5 Millimeter |
Catheter Working Length | 105 Centimeter |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00850291007215 [Primary] |
QEW | Peripheral Mechanical Thrombectomy With Aspiration |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2021-03-17 |
Device Publish Date | 2021-03-09 |
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