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: Sales Stripper Paddle, Drysdale/Sinskey, Double Ended, Reverse Drysdale, Lightly Textured Surface, Angled 10mm from Bend to Tip, Reverse Terry Sinskey Hook, Angled 15mm from Bend to Tip, Round Knurled Stainless Steel Handle, Overall Length 5.7" (145mm) FDA UDI
Model / Reference: 5-4238 FDA UDI
Description: Sales Stripper Paddle, Drysdale/Sinskey, Double Ended, Reverse Drysdale, Lightly Textured Surface, Angled 10mm from Bend to Tip, Reverse Terry Sinskey Hook, Angled 15mm from Bend to Tip, Round Knurled Stainless Steel Handle, Overall Length 5.7" (145mm) FDA UDI

Identifiers

Primary DI / UDI-DI: 00194613086459 FDA UDI
FDA Product Code: HNQ 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

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

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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 1e003298-9681-4937-ba36-255c2accc3ee 34 fields · synced May 30, 2026