Catalog Number

72200568F

Brand Name

500XL

Version/Model Number

72200568F

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

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

-

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

-

FDA Premarket Submission

-

Product Code

FFS

Product Code Name

image, illumination, fiberoptic, for endoscope

Public Device Record Key

d69b1b28-d3e5-4867-ac44-b3a78ee121a8

Public Version Date

March 29, 2018

Public Version Number

2

DI Record Publish Date

June 15, 2017

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-