EndoRings - The EndoRings is intended to be attached to the - ENDOAID LTD

Duns Number:600318101

Device Description: The EndoRings is intended to be attached to the distal end of the endoscope to facilitate The EndoRings is intended to be attached to the distal end of the endoscope to facilitate endoscopic therapy, to be used for the following: Keeping the suitable depth of endoscope's view field.

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More Product Details

Catalog Number

-

Brand Name

EndoRings

Version/Model Number

E103

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

Product Characteristics

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 Details

Product Code

FED

Product Code Name

Endoscopic Access Overtube, Gastroenterology-Urology

Device Record Status

Public Device Record Key

799ad9c4-3359-45b6-b89b-6d599732b14d

Public Version Date

March 29, 2018

Public Version Number

2

DI Record Publish Date

September 27, 2016

Additional Identifiers

Package DI Number

17290016767039

Quantity per Package

15

Contains DI Package

07290016767032

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

White carton box