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ReSolve ConvertX®

FDA UDI

Class II (US FDA UDI)

by Merit Medical Systems, Inc.

Identity

Trade Name
ReSolve ConvertX® FDA UDI
Generic Name
Polymeric ureteral stent FDA UDI
Model / Reference
00884450453193 FDA UDI

Identifiers

Catalog Number
RCX28-8-038 FDA UDI
Primary DI / UDI-DI
00884450453193 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

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI
MRI Safety
MR Conditional FDA UDI

Category: Polymeric ureteral stent

ReSolve ConvertX is a durable, flexible, and minimally invasive ureteral stent designed to promote urine flow in obstructed ureters. This medical device is intended for temporary implantation to improve renal pelvis to bladder drainage.

Similar devices

Also classified as Polymeric ureteral stent.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Merit Medical Systems, Inc.

Sources (1)

  • FDA UDI 3edb2ec7-db2d-4c9c-b1b7-06ae154b7643 33 fields · synced Jul 15, 2026