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: Lens loop, reusable FDA UDI
Device Name: Knolle-Pearce Irrigating Lens Loop, 23ga Thin Wall Shaft, 6mm Wide x 9mm Long Loop, Three Irrigating Ports At 12, 10, 2 O'Clock, Overall Length 1-1/2" (38mm) FDA UDI
Model / Reference: 5-1742 FDA UDI
Description: Knolle-Pearce Irrigating Lens Loop, 23ga Thin Wall Shaft, 6mm Wide x 9mm Long Loop, Three Irrigating Ports At 12, 10, 2 O'Clock, Overall Length 1-1/2" (38mm) FDA UDI

Identifiers

Primary DI / UDI-DI: 00194613104023 FDA UDI
FDA Product Code: HNQ FDA UDI
GMDN Term: Lens loop, 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

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Prescription Use

Yes

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Over-the-Counter

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Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

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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: Lens loop, 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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WILDER LENS LOOP — SONTEC INSTRUMENTS, 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 ca85a6ab-5592-4f36-8011-ba9904e2a911 34 fields · synced May 30, 2026