FDA UDI In Commercial Distribution 🇺🇸 United States

Pioneer Plus Catheter

DI: 00845225003425 · Model: PPLUS120 · Philips Image Guided Therapy Corporation
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Let the assistant research this device

The Research Assistant compiles product codes, classification, clearances and adverse events for this device — and cites every record.

Free to try · every answer cites its records

Basic Information

Brand Name
Pioneer Plus Catheter
Primary DI
00845225003425
Version / Model
PPLUS120
Catalog Number
PPLUS120
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
2024-08-12
Public Version
1
Public Version Date
2024-08-20
Public Version Status
New
Public Device Record Key
dd6fc5b2-340b-4e4c-a1cb-1bfe27110f73

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
Yes
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
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
ITX Transducer, Ultrasonic, Diagnostic
PDU Catheter For Crossing Total Occlusions

GMDN Terms

Code Name
44141 Intravascular ultrasound imaging catheter, single-use

Identifiers

Type ID
Primary 00845225003425

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K162418 000

Device Sizes

Type Value Unit Text
Length 120 Centimeter

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Keep dry
Type
Special Storage Condition, Specify
Special Conditions
Keep away from sunlight