V. Mueller

FDA UDI

Class I (US FDA UDI)

by Steris Corporation

Identity

Trade Name: V. Mueller FDA UDI
Generic Name: Eye spud FDA UDI
Device Name: V. Mueller ELLIS FOREIGN BODY SPUD, SMALL, CURVED ROUNDED BLADE, FLAT HANDLE, OVERALL LENGTH 4-1/2 inches FDA UDI
Model / Reference: OP0919-121 FDA UDI
Description: V. Mueller ELLIS FOREIGN BODY SPUD, SMALL, CURVED ROUNDED BLADE, FLAT HANDLE, OVERALL LENGTH 4-1/2 inches FDA UDI

Identifiers

Catalog Number: OP0919121 FDA UDI
Primary DI / UDI-DI: 10885403094927 FDA UDI
FDA Product Code: HNN FDA UDI
GMDN Term: Eye spud FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 886.4350 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Eye spud

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

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Also classified as Eye spud.

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Spud — Katena Products, Inc. · Class I
Spud — Katena Products, Inc. · Class I
Novo Surgical Inc. — NOVO SURGICAL, INC. · Class I
Integra® Miltex® — Integra LifeSciences Production Corporation · Class I

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Steris Corporation

Sources (1)

FDA UDI 94c1c353-079c-43fe-b872-793abdc67970 35 fields · synced Jun 8, 2026