Catalog Number

-

Brand Name

DeRoyal

Version/Model Number

NP-1002

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)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

-

Product Code

KDQ

Product Code Name

BOTTLE, COLLECTION, VACUUM

Public Device Record Key

ef1ad3f7-07d3-474d-8ebf-dfcbea3a758e

Public Version Date

August 10, 2021

Public Version Number

2

DI Record Publish Date

June 04, 2018

Package DI Number

50749756780976

Quantity per Package

10

Contains DI Package

00749756780971

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Case