Supracor Stimulite Honeycomb - Supracor, Inc.

Duns Number:118163781

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More Product Details

Catalog Number

-

Brand Name

Supracor Stimulite Honeycomb

Version/Model Number

SMXS1417

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

October 07, 2022

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

IMP

Product Code Name

Cushion, Wheelchair

Device Record Status

Public Device Record Key

bf51346f-5662-4b5a-a486-ef7a605b76e4

Public Version Date

October 14, 2022

Public Version Number

1

DI Record Publish Date

October 06, 2022

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"SUPRACOR, INC." Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 802