FDA UDI In Commercial Distribution 🇺🇸 United States

Trilogy Delivery Catheter

DI: 00850000898134 · Model: TRILOGY-DC-S · Jenavalve Technology, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Trilogy Delivery Catheter
Primary DI
00850000898134
Version / Model
TRILOGY-DC-S
Catalog Number
TRILOGY-DC-S
Company Name
Jenavalve Technology, Inc.
Labeler DUNS
827951620
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2026-03-25
Public Version
1
Public Version Date
2026-04-02
Public Version Status
New
Public Device Record Key
f7fc5921-c197-4e01-af3d-c1254a702990

Device Description

Transfemoral Delivery Catheter, Size 23MM

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
Yes
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
NPT Aortic Valve, Prosthesis, Percutaneously Delivered

GMDN Terms

Code Name
17846 Vascular guide-catheter, single-use

Identifiers

Type ID
Primary 00850000898134

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify 23MM

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
These devices must be stored in a cool, dry place