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: Radiation/mechanical corneal shield, reusable FDA UDI
Device Name: DuoShield For Bilateral Lasik, Adjustable Elastic Strap, Latex Free, Grey Tinted Polycarbonate, Moisture Retention, Foam Lining, Box of 25 FDA UDI
Model / Reference: G975MT-25 FDA UDI
Description: DuoShield For Bilateral Lasik, Adjustable Elastic Strap, Latex Free, Grey Tinted Polycarbonate, Moisture Retention, Foam Lining, Box of 25 FDA UDI

Identifiers

Primary DI / UDI-DI: 00194613122584 FDA UDI
FDA Product Code: HOY FDA UDI
GMDN Term: Radiation/mechanical corneal shield, reusable FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 886.4750 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: Radiation/mechanical corneal shield, 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 dc158e96-a49f-4985-b704-d4989a5732c6 34 fields · synced Jun 1, 2026