FDA UDI In Commercial Distribution 🇺🇸 United States

Trious

DI: 06973356555422 · Model: 231A6DG · Shenzhen Trious Medical Technology Co., Ltd.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Trious
Primary DI
06973356555422
Version / Model
231A6DG
Company Name
Shenzhen Trious Medical Technology Co., Ltd.
Labeler DUNS
698045520
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2026-03-27
Public Version
1
Public Version Date
2026-04-06
Public Version Status
New
Public Device Record Key
92d564de-bc8f-4d3b-a00c-0ae7892fb8cf

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
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
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
FAD Stent, Ureteral

GMDN Terms

Code Name
58005 Polymeric ureteral stent

Identifiers

Type ID
Primary 06973356555422

Premarket Submissions

Submission Number Supplement Number
K243830 000