FDA UDI Not in Commercial Distribution 🇺🇸 United States

AltaTrack

DI: 00884838070950 · Model: AltaTrack Catheter Berenstein · Philips Medical Systems Nederland B.V.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
AltaTrack
Primary DI
00884838070950
Version / Model
AltaTrack Catheter Berenstein
Catalog Number
ATC55080BRN
Company Name
Philips Medical Systems Nederland B.V.
Labeler DUNS
413819707
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-01-21
Public Version
4
Public Version Date
2024-01-15
Public Version Status
Update
Public Device Record Key
e634dc3d-320e-42fc-9b51-800d238910b5
Distribution End Date
2023-12-20

Device Description

Angiographic catheter with FORS technology intended to deliver radiopaque media or lead a guidewire in endovascular procedures of the peripheral, aortic and aortic side branch vasculature.

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
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
DQO Catheter, Intravascular, Diagnostic

GMDN Terms

Code Name
10688 Angiographic catheter, single-use

Identifiers

Type ID
Primary 00884838070950

Premarket Submissions

Submission Number Supplement Number
K201081 000