Catalog Number

20325-301

Brand Name

ERBE

Version/Model Number

20325-301

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

K103696,K103696,K103696,K103696,K103696

Product Code

FEQ

Product Code Name

PUMP, AIR, NON-MANUAL, FOR ENDOSCOPE

Public Device Record Key

859bada2-aa95-47c8-a8f4-3e90c57ba351

Public Version Date

June 10, 2022

Public Version Number

6

DI Record Publish Date

December 15, 2016

Package DI Number

04050147013551

Quantity per Package

7

Contains DI Package

04050147012981

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Level: 1