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Woven Filiform Coude Tip

FDA UDI

Class I (US FDA UDI)

by C. R. Bard, Inc.

Identity

Trade Name
Woven Filiform Coude Tip FDA UDI
Generic Name
Urethral dilator, reusable FDA UDI
Device Name
Woven Filiform Coude Tip FDA UDI
Model / Reference
022304 FDA UDI
Description
Woven Filiform Coude Tip FDA UDI

Identifiers

Catalog Number
022304 FDA UDI
Primary DI / UDI-DI
00801741073236 FDA UDI
FDA Product Code
FBW 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

Yes

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

No

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

Dimensions & Sizes

Size
Catheter Gauge — 4 French FDA UDI
Length — 12.5 Inch FDA UDI

Category: Urethral dilator, reusable

Woven Filiform Coude Tip 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 742a5fb3-d12c-48cd-8292-868586526d0d 36 fields · synced Jun 6, 2026