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: Ophthalmic surgical probe, reusable FDA UDI
Device Name: Folden Femto Dissector, Double Ended, Both Ends Angled 40 Degrees, 0.7mm Spatula, Beveled Edges, Slightly Pointed Tip, 1.2mm Spatula, Beveled Edges, Slightly Blunted Tip, Round Knurled Stainless Steel Handle, Overall Length 4-1/2" (115mm) FDA UDI
Model / Reference: 9-21255-R FDA UDI
Description: Folden Femto Dissector, Double Ended, Both Ends Angled 40 Degrees, 0.7mm Spatula, Beveled Edges, Slightly Pointed Tip, 1.2mm Spatula, Beveled Edges, Slightly Blunted Tip, Round Knurled Stainless Steel Handle, Overall Length 4-1/2" (115mm) FDA UDI

Identifiers

Primary DI / UDI-DI: 00194613084578 FDA UDI
FDA Product Code: HND FDA UDI
GMDN Term: Ophthalmic surgical probe, 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

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Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

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Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

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Lot / Batch Number

Yes

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Serial Number

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Expiration Date

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Manufacturing Date

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Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Ophthalmic surgical probe, 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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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 f569c674-c866-4fd7-b7a4-5cf0cfebaff9 34 fields · synced May 30, 2026