Catalog Number

-

Brand Name

Heff Med

Version/Model Number

HM-D820

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

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

Yes

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

K101598,K101598

Product Code

KKX

Product Code Name

Drape, Surgical

Public Device Record Key

306c96ff-3f63-4b46-bdd4-453202b3e86e

Public Version Date

December 22, 2021

Public Version Number

3

DI Record Publish Date

June 18, 2019

Package DI Number

10850003355372

Quantity per Package

20

Contains DI Package

00850003355375

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Case