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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
Corneal bur system, battery-powered FDA UDI
Device Name
Round Diamond Burr, 5mm Wide, Overall Length 20.5mm FDA UDI
Model / Reference
11-0012 FDA UDI
Description
Round Diamond Burr, 5mm Wide, Overall Length 20.5mm FDA UDI

Identifiers

Primary DI / UDI-DI
00194613020019 FDA UDI
FDA Product Code
OHW FDA UDI
GMDN Term
Corneal bur system, battery-powered FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
886.4070 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: Corneal bur system, battery-powered

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 Corneal bur system, battery-powered.

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 24fb28db-aebc-4da3-8313-ba921b0d3a98 34 fields · synced May 31, 2026