Catalog Number

20325-214

Brand Name

ERBEFLO® 2

Version/Model Number

20325-214

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

OCX

Product Code Name

Endoscopic Irrigation/Suction System

Public Device Record Key

849cb841-10ce-483f-a5f1-233189e9bf91

Public Version Date

December 10, 2021

Public Version Number

1

DI Record Publish Date

December 02, 2021

Package DI Number

04065655000207

Quantity per Package

10

Contains DI Package

04065655000191

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Level 1