Catalog Number

-

Brand Name

SUPER SHEATH 2.1SUPER SHEATH 2.1

Version/Model Number

VS5510

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

January 29, 2021

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"

Yes

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

DYB

Product Code Name

INTRODUCER, CATHETER

Public Device Record Key

6221855d-c142-4828-a762-9b23fbcc19b4

Public Version Date

February 04, 2021

Public Version Number

6

DI Record Publish Date

February 18, 2017

Package DI Number

50884908129156

Quantity per Package

5

Contains DI Package

00884908129151

Package Discontinue Date

January 29, 2021

Package Status

Not in Commercial Distribution

Package Type

box