Catalog Number

JBP Nanocannula 23Gx50mm

Brand Name

JBP Nanocannula

Version/Model Number

FTMN23-50

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"

-

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

K092831,K092831,K092831

Product Code

FMI

Product Code Name

Needle, Hypodermic, Single Lumen

Public Device Record Key

fb1628d9-7851-4700-a172-a0693311e05d

Public Version Date

October 23, 2019

Public Version Number

2

DI Record Publish Date

September 22, 2019

Package DI Number

28809407786250

Quantity per Package

1200

Contains DI Package

18809407786253

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-