Catalog Number

-

Brand Name

Pasteur Pipette 3 mL

Version/Model Number

16202

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

K201213,K201213

Product Code

MQK

Product Code Name

Labware, Assisted Reproduction

Public Device Record Key

539be8a0-7382-4d86-8947-8f67564bd38e

Public Version Date

December 30, 2020

Public Version Number

1

DI Record Publish Date

December 22, 2020

Package DI Number

17350025914623

Quantity per Package

500

Contains DI Package

07350025914626

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-