Tria™ Firm

FDA UDI

Class II (US FDA UDI)

by Boston Scientific

Identity

Trade Name: Tria™ Firm FDA UDI
Generic Name: Polymeric ureteral stent FDA UDI
Device Name: Ureteral Stent w/o Side Holes 6Fx20CM FDA UDI
Model / Reference: M0061902700 FDA UDI
Description: Ureteral Stent w/o Side Holes 6Fx20CM FDA UDI

Identifiers

Primary DI / UDI-DI: 08714729938118 FDA UDI
FDA Product Code: FAD FDA UDI
GMDN Term: Polymeric ureteral stent FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 876.4620 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

MRI Safety

MR Safe FDA UDI

Dimensions & Sizes

Size: Stent Diameter — 2.0 Millimeter FDA UDI
Shaft Length — 20 Centimeter FDA UDI

Category: Polymeric ureteral stent

Tria™ Firm by Boston Scientific — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Also classified as Polymeric ureteral stent.

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Universa — Cook, Inc. · Class II
Bard® InLay Optima® Ureteral Stent — C. R. Bard, Inc. · Class II
Bard® Fluoro-4™ Silicone Ureteral Coil Stent — C. R. Bard, Inc. · Class II
Porges Coloplast — Coloplast A/S · Class II

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Boston Scientific

Sources (1)

FDA UDI abcabd37-69cd-4490-b8a7-cb93b326ba21 34 fields · synced May 31, 2026