Catalog Number

-

Brand Name

AAP402-01 - MICROBORE YELLOW MARKED WITH NON-VENTED SPIKE

Version/Model Number

12004-000-0008

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)

Yes

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

K141389,K141389

Product Code

FPA

Product Code Name

Set, Administration, Intravascular

Public Device Record Key

666cd94d-197e-4e83-b1ca-855994ac6063

Public Version Date

June 20, 2019

Public Version Number

1

DI Record Publish Date

June 12, 2019

Package DI Number

27290109159298

Quantity per Package

30

Contains DI Package

17290109159291

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Cardboard box