Fiber Optic Light Guide - Fiber optic light probe for intraocular - ESCALON MEDICAL CORP.

Duns Number:879144426

Device Description: Fiber optic light probe for intraocular illumination with tissue manipulation. 45 degree Fiber optic light probe for intraocular illumination with tissue manipulation. 45 degree Retinal Knife, 20 ga, with TREK/Greishaber connector. Sterile,single-use.

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More Product Details

Catalog Number

TR9806-61

Brand Name

Fiber Optic Light Guide

Version/Model Number

45° Retinal Knife, TREK/Greishaber

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

Product Characteristics

MRI safety Status

Labeling does not contain MRI Safety Information

Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437)

-

Device labeled as "Not made with natural rubber latex"

-

For Single-Use

Yes

Prescription Use (Rx)

Yes

Over the Counter (OTC)

-

Kit

-

Combination Product

-

Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)

-

FDA Premarket Submission

K875195,K875195

Product Code Details

Product Code

FST

Product Code Name

Light, Surgical, Fiberoptic

Device Record Status

Public Device Record Key

8fb86ff4-fdd9-4787-9331-4cd7aba7118f

Public Version Date

May 07, 2019

Public Version Number

4

DI Record Publish Date

January 14, 2016

Additional Identifiers

Package DI Number

10853480006072

Quantity per Package

5

Contains DI Package

00853480006075

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Box

"ESCALON MEDICAL CORP." Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 5
2 A medical device with a moderate to high risk that requires special controls. 12