Catalog Number

-

Brand Name

Premium Plus

Version/Model Number

N055LAV

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

MDM

Product Code Name

Instrument, Manual, Surgical, General Use

Public Device Record Key

36b535a0-3623-4605-bfad-09aae17b1974

Public Version Date

February 06, 2020

Public Version Number

2

DI Record Publish Date

January 08, 2020

Package DI Number

D838N055LAV8

Quantity per Package

100

Contains DI Package

D838N055LAV2

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

CASE