Silhouette® Pediatric Ureteral Stent with Urowire® Guidewire

FDA UDI

Class II (US FDA UDI)

by Applied Medical Resources Corp.

Identity

Trade Name: Silhouette® Pediatric Ureteral Stent with Urowire® Guidewire FDA UDI
Generic Name: Polymeric ureteral stent FDA UDI
Device Name: Designed for patients 2 years and older for Temporary indwelling ureteral catheter to assist in urine drainage FDA UDI
Model / Reference: B3885 FDA UDI
Description: Designed for patients 2 years and older for Temporary indwelling ureteral catheter to assist in urine drainage FDA UDI

Identifiers

Primary DI / UDI-DI: 00607915113131 FDA UDI
FDA Product Code: KNY FDA UDI
EZB FDA UDI
FAD FDA UDI
GMDN Term: Polymeric ureteral stent FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 876.5130 FDA UDI
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 Conditional FDA UDI

Dimensions & Sizes

Size: Length — 12 Centimeter FDA UDI
Catheter Gauge — 4 French FDA UDI

Category: Polymeric ureteral stent

Silhouette® Pediatric Ureteral Stent with Urowire® Guidewire by Applied Medical Resources Corp. — Class II — FDA UDI — listed in FDA GUDID

Similar devices

Also classified as Polymeric ureteral stent.

Polaris™ Loop — Boston Scientific · Class II
Percuflex™ Plus — Boston Scientific · Class II
Percuflex™ Plus — Boston Scientific · Class II
Polaris™ Ultra — Boston Scientific · Class II
Q UROLOGICAL PERSISTENT AGUAMEDICINA — Q Urological Corporation · Class II
Universa — COOK INCORPORATED · Class II
Porges Coloplast — Coloplast A/S · Class II
TECOFLEX — Gyrus Acmi, Inc. · 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: Applied Medical Resources Corp.

Sources (1)

FDA UDI 4c266bd7-fe3a-4dff-9887-6b2139f34b60 35 fields · synced May 31, 2026