Catalog Number

G-260-2545A

Brand Name

VISIGLIDE2

Version/Model Number

G-260-2545A

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

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

OCY

Product Code Name

Endoscopic guidewire, gastroenterology-urology

Public Device Record Key

f57ab2d7-b1c1-4deb-acbd-543657268d2c

Public Version Date

July 14, 2022

Public Version Number

4

DI Record Publish Date

September 09, 2016

Package DI Number

54953170358246

Quantity per Package

5

Contains DI Package

04953170358241

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Carton