Catalog Number

20325-302

Brand Name

ERBE

Version/Model Number

20325-302

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

2c24d78b-4a54-477a-a6f0-e80ca89f821a

Public Version Date

April 23, 2019

Public Version Number

6

DI Record Publish Date

December 15, 2016

Package DI Number

04050147013575

Quantity per Package

7

Contains DI Package

04050147012998

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Level: 1