IDESIGN RS - KIT, ABR UPGRADE, IDESIGN RS, US - JOHNSON & JOHNSON SURGICAL VISION, INC.

Duns Number:010130626

Device Description: KIT, ABR UPGRADE, IDESIGN RS, US

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More Product Details

Catalog Number

0110-3451

Brand Name

IDESIGN RS

Version/Model Number

G301

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

-

Prescription Use (Rx)

Yes

Over the Counter (OTC)

-

Kit

-

Combination Product

Yes

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

-

FDA Premarket Submission

P930016

Product Code Details

Product Code

LZS

Product Code Name

Excimer laser system

Device Record Status

Public Device Record Key

5d951e0f-c5cb-47ba-a4fd-26b497b4e2c8

Public Version Date

May 04, 2022

Public Version Number

3

DI Record Publish Date

August 15, 2018

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"JOHNSON & JOHNSON SURGICAL VISION, INC." Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 42
2 A medical device with a moderate to high risk that requires special controls. 77
3 A medical device with high risk that requires premarket approval 3950