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Bard® InLay Optima® Ureteral Stent

FDA UDI

Class II (US FDA UDI)

by C. R. Bard, Inc.

Identity

Trade Name
Bard® InLay Optima® Ureteral Stent FDA UDI
Generic Name
Polymeric ureteral stent FDA UDI
Device Name
INLAY OPTIMA URETERAL STENT W/O GUIDEWIRE FDA UDI
Model / Reference
788430 FDA UDI
Description
INLAY OPTIMA URETERAL STENT W/O GUIDEWIRE FDA UDI

Identifiers

Catalog Number
788430 FDA UDI
Primary DI / UDI-DI
00801741015700 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

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

Dimensions & Sizes

Size
Catheter Gauge — 4.7 French FDA UDI
Length — 30 Centimeter FDA UDI

Category: Polymeric ureteral stent

Bard® InLay Optima® Ureteral Stent by C. R. Bard, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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
C. R. Bard, Inc.

Sources (1)

  • FDA UDI 3e72cca3-0a53-4b1e-82bf-99a56d8b062d 36 fields · synced Jun 8, 2026