Catalog Number

-

Brand Name

Portex

Version/Model Number

24-1015-64

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

K172823,K172823

Product Code

BSP

Product Code Name

NEEDLE, CONDUCTION, ANESTHETIC (W/WO INTRODUCER)

Public Device Record Key

ccb8d679-6be5-453f-9826-e8372e964452

Public Version Date

March 17, 2020

Public Version Number

1

DI Record Publish Date

March 09, 2020

Package DI Number

35019517079139

Quantity per Package

10

Contains DI Package

15019517079135

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Case