Catalog Number

682059

Brand Name

CRITIFLO(TM) TA1017 (3ML/HR)

Version/Model Number

682059

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

-

Product Code

DRS

Product Code Name

Transducer, Blood-Pressure, Extravascular

Public Device Record Key

9158f3f5-ac0c-468f-bdd1-06fa0213d4f8

Public Version Date

June 11, 2018

Public Version Number

3

DI Record Publish Date

September 30, 2016

Package DI Number

50886333620598

Quantity per Package

100

Contains DI Package

00886333620593

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Tyvek Pouch