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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
00884450453186 FDA UDI

Identifiers

Catalog Number
RCX26-8-038 FDA UDI
Primary DI / UDI-DI
00884450453186 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, easy-to-use ureteral stent for obstructed ureters. Made from synthetic polymer(s), it allows urine to drain from the renal pelvis to the bladder while maintaining luminal patency.

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 63b15d4f-ca5f-4d2a-b181-44a01211940a 33 fields · synced Jul 13, 2026