Catalog Number

22-267-410

Brand Name

Fisherbrand Serum Filter

Version/Model Number

IB Model

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

GIM

Product Code Name

Tubes, Vacuum Sample, With Anticoagulant

Public Device Record Key

fe8fdeff-3c0b-4091-b38d-54745028294c

Public Version Date

November 10, 2021

Public Version Number

3

DI Record Publish Date

September 14, 2016

Package DI Number

20817139020502

Quantity per Package

40

Contains DI Package

10817139020505

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-