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Bard® Goodwin Sounds

FDA UDI

Class I (US FDA UDI)

by C. R. Bard, Inc.

Identity

Trade Name
Bard® Goodwin Sounds FDA UDI
Generic Name
Urethral dilator, reusable FDA UDI
Device Name
Bard Goodwin Urethral Sound Complete Set 12 thru 30 Fr., Non-Sterile FDA UDI
Model / Reference
042800 FDA UDI
Description
Bard Goodwin Urethral Sound Complete Set 12 thru 30 Fr., Non-Sterile FDA UDI

Identifiers

Catalog Number
042800 FDA UDI
Primary DI / UDI-DI
00801741047213 FDA UDI
FDA Product Code
FBX FDA UDI
GMDN Term
Urethral dilator, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
876.5520 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Urethral dilator, reusable

Bard® Goodwin Sounds by C. R. Bard, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Urethral dilator, reusable.

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 fcf3039f-3774-47fc-a185-ac5f3054d3dd 35 fields · synced May 30, 2026