MSI Precision Specialty Instruments

FDA UDI

Class II (US FDA UDI)

by Med Saver, Inc.

Identity

Trade Name: MSI Precision Specialty Instruments FDA UDI
Generic Name: Ophthalmic sponge FDA UDI
Device Name: Lasik Pure Drain, 10.5mm Round Hole In Oval, 40mm Long x 14mm Wide, 1 Per Pouch, 20 Pouches Per Box (20 Units) FDA UDI
Model / Reference: 18-424 FDA UDI
Description: Lasik Pure Drain, 10.5mm Round Hole In Oval, 40mm Long x 14mm Wide, 1 Per Pouch, 20 Pouches Per Box (20 Units) FDA UDI

Identifiers

Primary DI / UDI-DI: 00194613100070 FDA UDI
FDA Product Code: HOZ FDA UDI
GMDN Term: Ophthalmic sponge FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 886.4790 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Manufacturing Date

FDA UDI

Category: Ophthalmic sponge

MSI Precision Specialty Instruments by Med Saver, Inc. — Class II — 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 II	Pending data

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Manufacturer

Manufacturer: Med Saver, Inc.

Sources (1)

FDA UDI 2aef0c21-2fc3-47a0-968a-f2232aa54c76 34 fields · synced Jun 8, 2026