FDA UDI In Commercial Distribution 🇺🇸 United States

Trevo NXT

DI: 07613327299922 · Model: 90312 · Stryker Corporation
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Trevo NXT
Primary DI
07613327299922
Version / Model
90312
Catalog Number
90312
Company Name
Stryker Corporation
Labeler DUNS
042405446
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-04-20
Public Version
4
Public Version Date
2022-11-09
Public Version Status
Update
Public Device Record Key
1b311505-fdae-4e1b-93b0-cf99d29fa3e3

Device Description

ProVue Retriever

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
NRY CATHETER, THROMBUS RETRIEVER
POL Neurovascular Mechanical Thrombectomy Device for Acute Ischemic Stroke Treatment

GMDN Terms

Code Name
58173 Thrombectomy suction catheter

Identifiers

Type ID
Primary 07613327299922

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify Distal Length: 25.0 Millimeter
Device Size Text, specify Stent Outer Diameter: 3.0 Millimeter
Device Size Text, specify Stent Length: 32.0 Millimeter

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Store in cool, dry, dark place.