Catalog Number

-

Brand Name

DRIVEMEDICAL

Version/Model Number

770-540

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

-

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

ILS

Product Code Name

ADAPTOR, HYGIENE

Public Device Record Key

270d46cf-24da-40e8-a02e-d3cb24d15474

Public Version Date

July 01, 2019

Public Version Number

1

DI Record Publish Date

June 21, 2019

Package DI Number

00057565993988

Quantity per Package

2

Contains DI Package

00775757705408

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-