Catalog Number

-

Brand Name

Drive

Version/Model Number

12132RF

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)

Yes

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

0924de5b-d8ce-420a-94b3-3c93ce10f785

Public Version Date

March 29, 2018

Public Version Number

2

DI Record Publish Date

July 10, 2017

Package DI Number

50822383536267

Quantity per Package

6

Contains DI Package

00822383536262

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-