FDA UDI Not in Commercial Distribution 🇺🇸 United States

AngioTouch® Kit

DI: 10841716100786 · Model: 014645 · ACIST MEDICAL SYSTEMS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
AngioTouch® Kit
Primary DI
10841716100786
Version / Model
014645
Company Name
ACIST MEDICAL SYSTEMS, INC.
Labeler DUNS
926684994
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-09
Public Version
4
Public Version Date
2022-09-16
Public Version Status
Update
Public Device Record Key
ad1d502c-5562-4101-bb68-1768ce2afb53
Distribution End Date
2018-05-21

Device Description

Model AT P65, p/n 701564-002 Kit Contents: hand controller, 3-way high-pressure stopcock with rotating end and premium high-pressure tubing

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
DXT Injector And Syringe, Angiographic

GMDN Terms

Code Name
47260 Contrast medium injection system hand controller kit

Identifiers

Type ID
Package 30841716100780
Primary 10841716100786