Catalog Number

-

Brand Name

Adapter Set for flexible endoscopes

Version/Model Number

ASP2

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)

-

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

-

Product Code

JRJ

Product Code Name

Unit, Drying

Public Device Record Key

0fc92ac3-9c4d-4022-9163-ac7d3e820014

Public Version Date

June 10, 2022

Public Version Number

2

DI Record Publish Date

September 24, 2020

Package DI Number

10843356102236

Quantity per Package

120

Contains DI Package

00843356102239

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-