Catalog Number

-

Brand Name

BOEHRINGER® ViSiGi 3D® Calibration System size 36Fr Bypass/Short

Version/Model Number

5236S

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"

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

K130483,K130483,K130483

Product Code

KNT

Product Code Name

Tubes, Gastrointestinal (And Accessories)

Public Device Record Key

92e5e843-55a6-4b86-b77a-0702612bfde1

Public Version Date

April 02, 2021

Public Version Number

2

DI Record Publish Date

July 01, 2018

Package DI Number

30816286020837

Quantity per Package

5

Contains DI Package

10816286020833

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Box