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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
Gonioscope FDA UDI
Device Name
Hwang-Latina 5 SLT Gonio Laser Lens, Flange, Contact Diameter 18mm, Lens Height 25mm, FOV 130 Degrees FDA UDI
Model / Reference
OHLSLTF FDA UDI
Description
Hwang-Latina 5 SLT Gonio Laser Lens, Flange, Contact Diameter 18mm, Lens Height 25mm, FOV 130 Degrees FDA UDI

Identifiers

Primary DI / UDI-DI
00194613121846 FDA UDI
FDA Product Code
HKS FDA UDI
GMDN Term
Gonioscope FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
886.1660 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: Gonioscope

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 Gonioscope.

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 a950ec01-7c19-469b-98d5-572992817d3a 34 fields · synced May 30, 2026