HD LenZ Pack for ZEISS RESIGHT® - 1 Each 54416 HD LenZ for ZEISS RESIGHT® & 1 Each - OCULUS SURGICAL INC

Duns Number:015409582

Device Description: 1 Each 54416 HD LenZ for ZEISS RESIGHT® & 1 Each 40417 Hassan-Tornambe Contact Lens

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More Product Details

Catalog Number

54010

Brand Name

HD LenZ Pack for ZEISS RESIGHT®

Version/Model Number

54010

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"

Yes

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

-

Product Code Details

Product Code

LRO

Product Code Name

General Surgery Tray

Device Record Status

Public Device Record Key

e26e5521-73b2-4a54-850b-34433063eaef

Public Version Date

June 17, 2022

Public Version Number

3

DI Record Publish Date

November 24, 2020

Additional Identifiers

Package DI Number

00852475007110

Quantity per Package

12

Contains DI Package

00852475007103

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Case

"OCULUS SURGICAL INC" Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 9
2 A medical device with a moderate to high risk that requires special controls. 8