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Councill Stylet

FDA UDI

Class I (US FDA UDI)

by C. R. Bard, Inc.

Identity

Trade Name
Councill Stylet FDA UDI
Generic Name
Urethral dilator, reusable FDA UDI
Device Name
Councill Stylet FDA UDI
Model / Reference
000437 FDA UDI
Description
Councill Stylet FDA UDI

Identifiers

Catalog Number
000437 FDA UDI
Primary DI / UDI-DI
00801741049019 FDA UDI
FDA Product Code
EZB FDA UDI
GMDN Term
Urethral dilator, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
876.5130 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

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
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Dimensions & Sizes

Size
Catheter Gauge — 6 French FDA UDI

Category: Urethral dilator, reusable

Councill Stylet 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 59388514-4a90-40a2-ac70-82addc9333f1 36 fields · synced May 29, 2026