FDA UDI In Commercial Distribution 🇺🇸 United States

CORE Mobile System

DI: 00845225012274 · Model: 400-0100.07 · Philips Image Guided Therapy Corporation
Product Codes
3
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
CORE Mobile System
Primary DI
00845225012274
Version / Model
400-0100.07
Catalog Number
400-0100.07
Company Name
Philips Image Guided Therapy Corporation
Labeler DUNS
018860556
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-12
Public Version
6
Public Version Date
2023-07-28
Public Version Status
Update
Public Device Record Key
3905475b-778b-4608-baba-6cd185e90a95

Device Description

CORE Mobile System - 240V

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
Yes
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
IYO System, Imaging, Pulsed Echo, Ultrasonic
DSK Computer, Blood-Pressure
DSA Cable, Transducer And Electrode, Patient, (Including Connector)

GMDN Terms

Code Name
40763 Cardiovascular ultrasound imaging system

Identifiers

Type ID
Primary 00845225012274

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K123898 000