Medline - MATTRESS,EQAIRE PLUS 12000,42X84X7, AG - MEDLINE INDUSTRIES, INC.

Duns Number:025460908

Device Description: MATTRESS,EQAIRE PLUS 12000,42X84X7, AG

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More Product Details

Catalog Number

MDTEP124284A

Brand Name

Medline

Version/Model Number

MDTEP124284A

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"

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 Details

Product Code

FNM

Product Code Name

MATTRESS, AIR FLOTATION, ALTERNATING PRESSURE

Device Record Status

Public Device Record Key

10a9e187-277b-4cc6-933d-35e5bc9a8187

Public Version Date

March 14, 2022

Public Version Number

1

DI Record Publish Date

March 04, 2022

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"MEDLINE INDUSTRIES, INC." Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 38540
2 A medical device with a moderate to high risk that requires special controls. 85094
3 A medical device with high risk that requires premarket approval 2
U Unclassified 7