AngioTouch® Kit - Model AT P65, p/n 701564-010Kit Contents: hand - ACIST MEDICAL SYSTEMS, INC.

Duns Number:926684994

Device Description: Model AT P65, p/n 701564-010Kit Contents: hand controller, 3-way high-pressure stopcock wi Model AT P65, p/n 701564-010Kit 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

014645

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

27abe547-dbba-46e7-a56c-a697a3a0bb10

Public Version Date

September 16, 2022

Public Version Number

3

DI Record Publish Date

December 08, 2016

Additional Identifiers

Package DI Number

30841716101367

Quantity per Package

10

Contains DI Package

10841716101363

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Shelf box

"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