MSI Precision Specialty Instruments

FDA UDI

Class I (US FDA UDI)

by Med Saver, Inc.

Identity

Trade Name: MSI Precision Specialty Instruments FDA UDI
Generic Name: Eyelid speculum, reusable FDA UDI
Device Name: Lieberman-Brown Triple Post Eye Speculum, Small Double Wire Blades, Total Blade Width 16mm, 1mm Top Center Wire Blade, Adjustable Mechanism, Angled Down Towards Temple, Overall Length 3" (79mm) FDA UDI
Model / Reference: 11-2-6785 FDA UDI
Description: Lieberman-Brown Triple Post Eye Speculum, Small Double Wire Blades, Total Blade Width 16mm, 1mm Top Center Wire Blade, Adjustable Mechanism, Angled Down Towards Temple, Overall Length 3" (79mm) FDA UDI

Identifiers

Primary DI / UDI-DI: 00194613100476 FDA UDI
FDA Product Code: HNC FDA UDI
GMDN Term: Eyelid speculum, reusable 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: Eyelid speculum, reusable

MSI Precision Specialty Instruments by Med Saver, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Eyelid speculum, reusable.

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Ambler Surgical — Ambler Surgical, LLC · Class I
Walcott Rx Products — Walcott Rx Product Inc · Class I
COOK EYE SPECULUM — SONTEC INSTRUMENTS, INC. · Class I
Wire Speculum — SONTEC INSTRUMENTS, INC. · Class I
Visitec® — Beaver-Visitec International, Inc. · 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: Med Saver, Inc.

Sources (1)

FDA UDI 6681716f-1ab7-4b70-8128-c59c24458393 34 fields · synced May 30, 2026