Sechrist Industries, Inc. - STRETCHER W/STRCH.PLT - SECHRIST INDUSTRIES, INC.

Duns Number:062084215

Device Description: STRETCHER W/STRCH.PLT W/HEADREST&OMNIPRESS.WIDE,ENGL.3300H

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More Product Details

Catalog Number

-

Brand Name

Sechrist Industries, Inc.

Version/Model Number

21790-101-33H

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

FPO

Product Code Name

Stretcher, Wheeled

Device Record Status

Public Device Record Key

cca5cb35-afef-463b-80be-fe14d201c684

Public Version Date

March 29, 2018

Public Version Number

2

DI Record Publish Date

May 31, 2017

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"SECHRIST INDUSTRIES, INC." Characteristics
Device Class Device Class Description No of Devices
2 A medical device with a moderate to high risk that requires special controls. 169