FDA UDI In Commercial Distribution 🇺🇸 United States

Triever20

DI: 00850291007079 · Model: 21-101 · INARI MEDICAL INC
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Triever20
Primary DI
00850291007079
Version / Model
21-101
Company Name
INARI MEDICAL INC
Labeler DUNS
076827459
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-04-19
Public Version
6
Public Version Date
2022-11-09
Public Version Status
Update
Public Device Record Key
63f54d9d-f912-45ea-a925-828229a64fea

Device Description

Triever20 Catheter, Gen 4

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
QEW Peripheral Mechanical Thrombectomy With Aspiration
KRA Catheter, Continuous Flush

GMDN Terms

Code Name
58173 Thrombectomy suction catheter

Identifiers

Type ID
Primary 00850291007079

Customer Contacts

Phone
19496008433

Device Sizes

Type Value Unit Text
Outer Diameter 6.7 Millimeter