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V. Mueller

FDA UDI

Class I (US FDA UDI)

by Steris Corporation

Identity

Trade Name
V. Mueller FDA UDI
Generic Name
Filiform urethral bougie FDA UDI
Device Name
WIRE MANDRIN 8FR GUYON-BENIQUE CURVE OVERALL LENGTH 16-3/4 inches42.6CM FDA UDI
Model / Reference
GU3401 FDA UDI
Description
WIRE MANDRIN 8FR GUYON-BENIQUE CURVE OVERALL LENGTH 16-3/4 inches42.6CM FDA UDI

Identifiers

Catalog Number
GU3401 FDA UDI
Primary DI / UDI-DI
10885403048951 FDA UDI
FDA Product Code
EZB FDA UDI
GMDN Term
Filiform urethral bougie 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

Category: Filiform urethral bougie

V. Mueller by Steris Corporation — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Filiform urethral bougie.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Steris Corporation

Sources (1)

  • FDA UDI 94f7d277-e310-4939-8ef4-54218a4f7e0c 35 fields · synced Jun 6, 2026