Catalog Number

POUCH

Brand Name

ENDOPOUCH RETRIEVER

Version/Model Number

POUCH

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

GCJ

Product Code Name

Laparoscope, general & plastic surgery

Public Device Record Key

e8b5579f-6866-4aae-a7b8-2e5ca3cce76b

Public Version Date

October 16, 2019

Public Version Number

3

DI Record Publish Date

July 15, 2016

Package DI Number

30705036012980

Quantity per Package

18

Contains DI Package

10705036012986

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

CASE