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: Guyton-Park Speculum, Solid 14mm Blades, Dull Finish, 45mm Spread, Suture Posts, Canthus Bar, Overall Length 3-1/4" (82mm)_x000D_ FDA UDI
Model / Reference: 5-5112 FDA UDI
Description: Guyton-Park Speculum, Solid 14mm Blades, Dull Finish, 45mm Spread, Suture Posts, Canthus Bar, Overall Length 3-1/4" (82mm)_x000D_ FDA UDI

Identifiers

Primary DI / UDI-DI: 00194613064488 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

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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

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Also classified as Eyelid speculum, reusable.

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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 2de6ce6d-9dfa-4a97-8bee-721c3787146c 34 fields · synced May 30, 2026