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 knife, single-use FDA UDI
Device Name: Clear Control 3D Slit Knife, Angled, 1.8mm Blade, Micro Bevels, Less Stress on Wound Margins, 22% Thinner Blade, Full Handle, Sold Individually Sterile, 6 Blades Per Box FDA UDI
Model / Reference: 72-1850 FDA UDI
Description: Clear Control 3D Slit Knife, Angled, 1.8mm Blade, Micro Bevels, Less Stress on Wound Margins, 22% Thinner Blade, Full Handle, Sold Individually Sterile, 6 Blades Per Box FDA UDI

Identifiers

Primary DI / UDI-DI: 00194613018795 FDA UDI
FDA Product Code: HNN FDA UDI
GMDN Term: Ophthalmic knife, single-use 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

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 knife, single-use

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 knife, single-use.

MANI Ophthalmic Knife — MANI, INC. · Class I
Ophthalmic Knife — Katena Products, Inc. · Class I
MANI Ophthalmic Knife — MANI, INC. · Class I
MANI Ophthalmic Knife — MANI, INC. · Class I
MANI Ophthalmic Knife — MANI, INC. · Class I
Anodyne Surgical — Psi/Eye-Ko, Inc. · Class I
MANI Ophthalmic Knife — MANI, INC. · Class I
Premier Edge® Microsurgical Knives — OASIS 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 893550b9-ead4-4c7c-9c46-053ca10163b9 34 fields · synced May 31, 2026