Catalog Number

-

Brand Name

Lot Fancy

Version/Model Number

330*38

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

-

Product Code

MQX

Product Code Name

Needle, Acupuncture, Single Use

Public Device Record Key

5ba410e7-b2ac-4bbc-9659-bdd8e2c1eaf8

Public Version Date

June 01, 2021

Public Version Number

1

DI Record Publish Date

May 24, 2021

Package DI Number

16972011716588

Quantity per Package

400

Contains DI Package

06972011716581

Package Discontinue Date

May 24, 2021

Package Status

Not in Commercial Distribution

Package Type

carton