ARROW - Pressure Injectable Arrowg+ard Blue Advance(R) - TELEFLEX INCORPORATED

Duns Number:002348191

Device Description: Pressure Injectable Arrowg+ard Blue Advance(R) One-Lumen PICC

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More Product Details

Catalog Number

CDC-45541-HPK1A

Brand Name

ARROW

Version/Model Number

IPN036773

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

Product Characteristics

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

K112896,K112896

Product Code Details

Product Code

LJS

Product Code Name

Catheter,intravascular,therapeutic,long-term greater than 30 days

Device Record Status

Public Device Record Key

cb8d0016-9838-4820-bc97-854f426cbc58

Public Version Date

December 15, 2021

Public Version Number

11

DI Record Publish Date

October 09, 2017

Additional Identifiers

Package DI Number

20801902124078

Quantity per Package

5

Contains DI Package

30801902124075

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Case

"TELEFLEX INCORPORATED" Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 3195
2 A medical device with a moderate to high risk that requires special controls. 13747
3 A medical device with high risk that requires premarket approval 3
U Unclassified 26