AngioTouch® Kit - Model AT P54, p/n 700608-055Kit Contents: hand - ACIST MEDICAL SYSTEMS, INC.

Duns Number:926684994

Device Description: Model AT P54, p/n 700608-055Kit Contents: hand controller, 3-way high-pressure stopcock wi Model AT P54, p/n 700608-055Kit Contents: hand controller, 3-way high-pressure stopcock with rotating end and premium high-pressure tubing

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More Product Details

Catalog Number

-

Brand Name

AngioTouch® Kit

Version/Model Number

014644

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"

-

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 Details

Product Code

DXT

Product Code Name

Injector And Syringe, Angiographic

Device Record Status

Public Device Record Key

c4b46419-8056-41e4-8513-752ae3f2cf00

Public Version Date

September 16, 2022

Public Version Number

2

DI Record Publish Date

May 06, 2019

Additional Identifiers

Package DI Number

30841716102135

Quantity per Package

10

Contains DI Package

10841716102131

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-

"ACIST MEDICAL SYSTEMS, INC." Characteristics
Device Class Device Class Description No of Devices
2 A medical device with a moderate to high risk that requires special controls. 193