Catalog Number

-

Brand Name

N/A

Version/Model Number

ED32-i10

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

FDT

Product Code Name

duodenoscope and accessories, flexible/rigid

Public Device Record Key

2f008ece-3934-48b3-b9cb-7f60fce51d00

Public Version Date

February 10, 2022

Public Version Number

1

DI Record Publish Date

February 02, 2022

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-