Catalog Number

-

Brand Name

Mobi-tools translide

Version/Model Number

TTE6102

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

MRI safety Status

MR Safe

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

FMR

Product Code Name

DEVICE, TRANSFER, PATIENT, MANUAL

Public Device Record Key

a73d4ff9-c550-4e16-9d1d-f2596de8cc52

Public Version Date

September 09, 2020

Public Version Number

2

DI Record Publish Date

November 22, 2019

Package DI Number

08436035357635

Quantity per Package

50

Contains DI Package

08436035357628

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-