Catalog Number

-

Brand Name

Eclipse DermaFlex MicroCannula

Version/Model Number

DF27G50MM26G

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)

Yes

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

K200017,K200017

Product Code

FMI

Product Code Name

Needle, Hypodermic, Single Lumen

Public Device Record Key

ce87225d-b44e-435c-b1be-0e31de01e7e4

Public Version Date

March 31, 2021

Public Version Number

1

DI Record Publish Date

March 23, 2021

Package DI Number

10853602008519

Quantity per Package

25

Contains DI Package

00853602008512

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Box