Catalog Number

-

Brand Name

NUNC IVF MULTIDISH 4 WELL NUNCLON

Version/Model Number

144444

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

-

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

PUD

Product Code Name

Labware, Assisted Reproduction, Exempt

Public Device Record Key

adf8dfa1-14c0-4f98-bc9a-20e323ed6d5b

Public Version Date

May 28, 2021

Public Version Number

3

DI Record Publish Date

September 21, 2018

Package DI Number

35713311000121

Quantity per Package

30

Contains DI Package

15713311000127

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Case