Catalog Number

2B8019

Brand Name

INTRAVIA

Version/Model Number

2B8019

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"

Yes

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

K964853,K964853,K964853

Product Code

KPE

Product Code Name

CONTAINER, I.V.

Public Device Record Key

6908a5a8-241c-4454-822d-df33ac1a771b

Public Version Date

October 23, 2019

Public Version Number

4

DI Record Publish Date

September 24, 2016

Package DI Number

50085412003509

Quantity per Package

48

Contains DI Package

20085412003508

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

CASE