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: Seibel Style Nucleus Chopper / Safety Quick Chopper, Double Ended, Use In LH, RH Dominant Surgeon, Seibel End, Curved Interior Cutting Edge, 0.5mm Olive Shaped Tip, 15mm From Bend To Tip, Safety Chopper End, 0.5mm Olive Shaped Blade, 1mm Bend, Angled 10mm From Bend To Tip, Stainless Steel, Overall Length 5-1/2" (140mm) FDA UDI
Model / Reference: 9-25647-RR FDA UDI
Description: Seibel Style Nucleus Chopper / Safety Quick Chopper, Double Ended, Use In LH, RH Dominant Surgeon, Seibel End, Curved Interior Cutting Edge, 0.5mm Olive Shaped Tip, 15mm From Bend To Tip, Safety Chopper End, 0.5mm Olive Shaped Blade, 1mm Bend, Angled 10mm From Bend To Tip, Stainless Steel, Overall Length 5-1/2" (140mm) FDA UDI

Identifiers

Primary DI / UDI-DI: 00194613018375 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

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

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

Similar devices

Also classified as Ophthalmic surgical probe, reusable.

Millennium — AVALIGN TECHNOLOGIES, Inc. · Class I
V. Mueller — STERIS CORPORATION · Class I
Millennium — AVALIGN TECHNOLOGIES, Inc. · Class I
Millennium — AVALIGN TECHNOLOGIES, Inc. · Class I
Titanium Nucleus Splitter — KATALYST SURGICAL, LLC · Class I
Scleral Depressors — AURORA SURGICAL, LLC · Class I
Medetz Surgical Instruments — MEDETZ SURGICAL INSTRUMENTS · Class I
Hayden Medical — Hayden Medical 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer: Med Saver, Inc.

Sources (1)

FDA UDI 00d6cc34-53b5-4c35-94fb-318acd0ccb10 34 fields · synced Jun 6, 2026