Promax OR Gowns - OR GWN PROMAX KAUM AQUA XL - RM (98 8282) USE: - STANDARD TEXTILE CO., INC.

Duns Number:006999858

Device Description: OR GWN PROMAX KAUM AQUA XL - RM (98 8282) USE: 7567P314

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More Product Details

Catalog Number

7567U694

Brand Name

Promax OR Gowns

Version/Model Number

7567U694

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)

Yes

Kit

-

Combination Product

-

Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)

-

FDA Premarket Submission

K041540,K041540

Product Code Details

Product Code

FYA

Product Code Name

Gown, Surgical

Device Record Status

Public Device Record Key

87616477-23ad-4e23-9c60-618d6d52ac8f

Public Version Date

April 07, 2021

Public Version Number

5

DI Record Publish Date

January 29, 2018

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"STANDARD TEXTILE CO., INC." Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 26
2 A medical device with a moderate to high risk that requires special controls. 9