FDA UDI In Commercial Distribution 🇺🇸 United States

Philips

DI: 00884838091122 · Model: 459801419352 · Philips Medical Systems (cleveland), Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Philips
Primary DI
00884838091122
Version / Model
459801419352
Catalog Number
459801419352
Company Name
Philips Medical Systems (cleveland), Inc.
Labeler DUNS
829526560
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-02-27
Public Version
1
Public Version Date
2020-03-06
Public Version Status
New
Public Device Record Key
9fc72ed9-ed46-49cc-a839-2d2de44c1137

Device Description

Pinnacle3 Radiation therapy treatment planning system version 16.2.1.60098

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

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
MUJ System, planning, radiation therapy treatment

GMDN Terms

Code Name
40887 Radiation therapy software

Identifiers

Type ID
Primary 00884838091122

Premarket Submissions

Submission Number Supplement Number
K170086 000