Drive - Patient RoomSlings Product Description: - Drive Devilbiss Healthcare

Duns Number:867673159

Device Description: Patient RoomSlings Product Description: Sling,Polystr.for Lift 1/bx

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More Product Details

Catalog Number

-

Brand Name

Drive

Version/Model Number

13025

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

Product Characteristics

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 Details

Product Code

FSA

Product Code Name

LIFT, PATIENT, NON-AC-POWERED

Device Record Status

Public Device Record Key

466fb00d-3af8-493f-bfdf-809dd67289af

Public Version Date

November 23, 2021

Public Version Number

4

DI Record Publish Date

July 10, 2017

Additional Identifiers

Package DI Number

50822383103315

Quantity per Package

24

Contains DI Package

00822383103310

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-

"DRIVE DEVILBISS HEALTHCARE" Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 3783
2 A medical device with a moderate to high risk that requires special controls. 832