Catalog Number

-

Brand Name

Premium Plus

Version/Model Number

205M-ASS

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In HIBCC

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)

-

Over the Counter (OTC)

-

Kit

-

Combination Product

-

Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)

-

FDA Premarket Submission

-

Product Code

GEA

Product Code Name

Cannula, Surgical, General & Plastic Surgery

Public Device Record Key

a68f62e9-aa9f-46f5-8003-870cce0b4d7b

Public Version Date

January 03, 2020

Public Version Number

1

DI Record Publish Date

December 26, 2019

Package DI Number

D838205MASS8

Quantity per Package

4

Contains DI Package

D838205MASS6

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

CASE