FDA UDI In Commercial Distribution 🇺🇸 United States

Delta4 Phantom+ MR

DI: 17350005180086 · Model: PW · Scandidos AB
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Delta4 Phantom+ MR
Primary DI
17350005180086
Version / Model
PW
Catalog Number
SDOS101-34
Company Name
Scandidos AB
Labeler DUNS
507639297
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-04-24
Public Version
1
Public Version Date
2019-05-02
Public Version Status
New
Public Device Record Key
3aea9646-c7ec-46d2-a860-d4f2d300cf7c

Device Description

The intended use of the device is • quality assurance of patient specific treatment delivery prior to the treatment in IMRT (including VMAT) and 4DRT (e.g. respiratory gating and tumour tracking). • quality assurance of the radiation delivery system.

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
MR Conditional
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
IYE Accelerator, Linear, Medical

GMDN Terms

Code Name
40624 Multi-modality therapeutic radiation phantom, anthropomorphic

Identifiers

Type ID
Primary 17350005180086

Customer Contacts

Phone
+46184723030

Premarket Submissions

Submission Number Supplement Number
K183606 000