Catalog Number

HMSLING-50RS-TVA-B

Brand Name

HoverSling Repositiong Sling-TVA

Version/Model Number

HMSLING-50RS-TVA-B

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

MRI safety Status

MR Conditional

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"

Yes

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

FRZ

Product Code Name

Device, Patient Transfer, Powered

Public Device Record Key

2573ac7d-6107-4dfe-9347-999def7168b6

Public Version Date

November 08, 2021

Public Version Number

1

DI Record Publish Date

October 29, 2021

Package DI Number

00816299010244

Quantity per Package

5

Contains DI Package

00816299010251

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

box