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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 curette, reusable FDA UDI
Device Name
Foreign Body Curette, Straight 31mm Shaft, 0.5mm Cup, Flat Handle, Polished Finish, Overall Length 5" (129mm) FDA UDI
Model / Reference
5-1918 FDA UDI
Description
Foreign Body Curette, Straight 31mm Shaft, 0.5mm Cup, Flat Handle, Polished Finish, Overall Length 5" (129mm) FDA UDI

Identifiers

Primary DI / UDI-DI
00194613075361 FDA UDI
FDA Product Code
HNZ FDA UDI
GMDN Term
Ophthalmic curette, 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

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Ophthalmic curette, 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 curette, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Med Saver, Inc.

Sources (1)

  • FDA UDI 4ab79797-63a0-4c2b-9b88-efeef21a733e 34 fields · synced Jun 1, 2026