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Bard® Push Catheter

FDA UDI

Class II (US FDA UDI)

by C. R. Bard, Inc.

Identity

Trade Name
Bard® Push Catheter FDA UDI
Generic Name
Ureteral stent-placement set FDA UDI
Device Name
Bard® Push Catheter FDA UDI
Model / Reference
888888 FDA UDI
Description
Bard® Push Catheter FDA UDI

Identifiers

Catalog Number
888888 FDA UDI
Primary DI / UDI-DI
00801741039225 FDA UDI
FDA Product Code
FAD FDA UDI
GMDN Term
Ureteral stent-placement set 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

Dimensions & Sizes

Size
Length — 45 Centimeter FDA UDI
Catheter Gauge — 4.7 French FDA UDI

Category: Ureteral stent-placement set

Bard® Push Catheter by C. R. Bard, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Ureteral stent-placement set.

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 dd67dcc0-94d2-4d1a-a466-937fb07ac149 36 fields · synced May 30, 2026