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Expel™ Ureteral Stent System

FDA UDI

Class II (US FDA UDI)

by Boston Scientific

Identity

Trade Name
Expel™ Ureteral Stent System FDA UDI
Generic Name
Nephrostomy catheter FDA UDI
Device Name
Ureteral Stent System FDA UDI
Model / Reference
H7493936106160 FDA UDI
Description
Ureteral Stent System FDA UDI

Identifiers

Catalog Number
H7493936106160 FDA UDI
Primary DI / UDI-DI
08714729861027 FDA UDI
FDA Product Code
FAD FDA UDI
GMDN Term
Nephrostomy catheter 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

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

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

No

FDA UDI
MRI Safety
MR Conditional FDA UDI

Category: Nephrostomy catheter

Expel™ Ureteral Stent System by Boston Scientific — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Nephrostomy catheter.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Boston Scientific

Sources (1)

  • FDA UDI e88e785f-c7b7-4485-9cf5-c5d7320e56ba 35 fields · synced Jun 1, 2026