FDA UDI In Commercial Distribution 🇺🇸 United States

Trevo

DI: 00815742002317 · Model: 90231 · Stryker Corporation
Product Codes
3
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Trevo
Primary DI
00815742002317
Version / Model
90231
Catalog Number
90231
Company Name
Stryker Corporation
Labeler DUNS
042405446
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-21
Public Version
4
Public Version Date
2021-01-11
Public Version Status
Update
Public Device Record Key
2e899e50-3853-45e4-b02f-64c19d19c78f

Device Description

Trevo Pro 14 Microcatheter

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
DQY CATHETER, PERCUTANEOUS
DQO CATHETER, INTRAVASCULAR, DIAGNOSTIC
KRA Catheter, continuous flush

GMDN Terms

Code Name
10688 Angiographic catheter, single-use

Identifiers

Type ID
Primary 00815742002317

Customer Contacts

Device Sizes

Type Value Unit Text
Length 157.0 Centimeter
Lumen/Inner Diameter 0.017 Inch

Storage Conditions

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