Catalog Number

85.921

Brand Name

Micro-Needle

Version/Model Number

85.921

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

JKA

Product Code Name

Tubes, Vials, Systems, Serum Separators, Blood Collection

Public Device Record Key

8203d284-9038-4448-a816-e3305fbb1640

Public Version Date

April 07, 2021

Public Version Number

5

DI Record Publish Date

September 16, 2016

Package DI Number

04038917315500

Quantity per Package

500

Contains DI Package

04038917315517

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-