Catalog Number

4892705NR-02

Brand Name

Stimuplex®

Version/Model Number

4892705NR-02

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

-

Product Code

BSP

Product Code Name

NEEDLE, CONDUCTION, ANESTHETIC (W/WO INTRODUCER)

Public Device Record Key

d186002b-3527-491c-bd0c-102d99b3782b

Public Version Date

February 11, 2022

Public Version Number

2

DI Record Publish Date

September 21, 2020

Package DI Number

04046955649372

Quantity per Package

18

Contains DI Package

04046955255399

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Carton