FDA UDI In Commercial Distribution 🇺🇸 United States

LumiGuide

DI: 00884838112087 · Model: LumiGuide Equipment · Philips Medical Systems Nederland B.V.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
LumiGuide
Primary DI
00884838112087
Version / Model
LumiGuide Equipment
Catalog Number
NCVC933
Company Name
Philips Medical Systems Nederland B.V.
Labeler DUNS
413819707
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-09-18
Public Version
2
Public Version Date
2024-02-23
Public Version Status
Update
Public Device Record Key
147b1f2d-489d-4199-b924-f5e02f6b55de

Device Description

Visualization device with FORS technology intended to aid the positioning and navigation of a connected AltaTrack Guidewire and optionally a catheter during endovascular procedures of the peripheral, aortic and aortic side branch vasculature, by creating a 3D image in real time of the connected AltaTrack Guidewire, and of an endovascular catheter, when combined with an AltaTrack 3D Hub.

Device Characteristics

Single Use
No
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
Yes
Has Lot/Batch Number
No
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
DQK Computer, Diagnostic, Programmable

GMDN Terms

Code Name
58473 Diagnostic x-ray digital imaging system workstation application software

Identifiers

Type ID
Primary 00884838112087

Premarket Submissions

Submission Number Supplement Number
K223918 000