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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
Hill Open Access Surgical Gonio Lens, Held in Left Hand, Increased Clearance To Clear Cornea, Surface Area 54mm, Gonio Magnification 1.2x, Field of View 90 Degrees, Handle Length 78mm FDA UDI
Model / Reference
OHSOG-LH FDA UDI
Description
Hill Open Access Surgical Gonio Lens, Held in Left Hand, Increased Clearance To Clear Cornea, Surface Area 54mm, Gonio Magnification 1.2x, Field of View 90 Degrees, Handle Length 78mm FDA UDI

Identifiers

Primary DI / UDI-DI
00194613121808 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 9c11a7da-a68f-4495-951a-b825c8fd39ea 34 fields · synced May 30, 2026